1-1     By:  Van de Putte, Wise (Senate Sponsor - Madla)      H.B. No. 1070

 1-2           (In the Senate - Received from the House May 7, 1997;

 1-3     May 8, 1997, read first time and referred to Committee on Criminal

 1-4     Justice; May 18, 1997, reported favorably, as amended, by the

 1-5     following vote:  Yeas 6, Nays 0; May 18, 1997, sent to printer.)

 1-6     COMMITTEE AMENDMENT NO. 1                            By:  Patterson

 1-7           Amend House Committee Report for HB1070 on page 11 line 2 by

 1-8     adding the following after the word "Commissioner":

 1-9     ", with the approval of the Texas Board of Health,".

1-10     COMMITTEE AMENDMENT NO. 2                             By:  Whitmire

1-11           Amend HB 1070 as follows:

1-12           Delete SECTION 25 and SECTION 26 and renumber subsequent

1-13     sections accordingly.

1-14                            A BILL TO BE ENTITLED

1-15                                   AN ACT

1-16     relating to drug regulation and enforcement under the Texas

1-17     Controlled Substances Act and to the authority of certain state

1-18     agencies under that Act and to certain penalties for the use of a

1-19     controlled substance to commit the offense; imposing criminal

1-20     penalties.

1-21           BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:

1-22           SECTION 1.  Section 481.002, Health and Safety Code, is

1-23     amended by amending Subdivisions (3), (4), (5), (6), (17), (30),

1-24     and (41) and by adding Subdivision (50) to read as follows:

1-25                 (3)  "Commissioner" means the commissioner of public

1-26     health or the commissioner's designee.

1-27                 (4)  "Controlled premises" means:

1-28                       (A)  a place where original or other records or

1-29     documents required under this chapter are kept or are required to

1-30     be kept; or

1-31                       (B)  a place, including a factory, warehouse,

1-32     other establishment, or conveyance, where a person registered under

1-33     this chapter may lawfully hold, manufacture, distribute, dispense,

1-34     administer, possess, or otherwise dispose of a controlled substance

1-35     or other item governed by this chapter, including a chemical

1-36     precursor and a chemical  laboratory apparatus.

1-37                 (5)  "Controlled substance" means a substance,

1-38     including a drug, an adulterant, a dilutant, and an immediate

1-39     precursor, listed in Schedules I  through V or Penalty Groups 1,

1-40     1-A, or 2 through 4.  The term includes the aggregate weight of any

1-41     mixture, solution, or other substance  containing a controlled

1-42     substance.

1-43                 (6)  "Controlled substance analogue" means:

1-44                       (A)  a substance with a chemical structure

1-45     substantially similar to the chemical structure of a controlled

1-46     substance in Schedule I or II or Penalty Group 1, 1-A, or 2; or

1-47                       (B)  a substance specifically designed to produce

1-48     an effect substantially similar to, or greater than, the effect of

1-49     a controlled substance in Schedule I or II or Penalty Group 1, 1-A,

1-50     or 2.

1-51                 (17)  "Drug paraphernalia" means equipment, a product,

1-52     or material that is used or intended for use in planting,

1-53     propagating, cultivating, growing, harvesting, manufacturing,

1-54     compounding, converting, producing, processing, preparing, testing,

1-55     analyzing, packaging, repackaging, storing, containing, or

1-56     concealing a controlled substance in violation of this chapter or

1-57     in  injecting, ingesting, inhaling, or otherwise introducing into

1-58     the human body a controlled substance in violation of this chapter.

1-59     The term includes:

1-60                       (A)  a kit used or intended for use in planting,

1-61     propagating, cultivating, growing, or harvesting a species of plant

1-62     that is a controlled  substance or from which a controlled

1-63     substance may be derived;

1-64                       (B)  a material, compound, mixture, preparation,

 2-1     or kit used or intended for use in manufacturing, compounding,

 2-2     converting, producing,  processing, or preparing a controlled

 2-3     substance;

 2-4                       (C)  an isomerization device used or intended for

 2-5     use in increasing the potency of a species of plant that is a

 2-6     controlled substance;

 2-7                       (D)  testing equipment used or intended for use

 2-8     in identifying or in analyzing the strength, effectiveness, or

 2-9     purity of a controlled substance;

2-10                       (E)  a scale or balance used or intended for use

2-11     in weighing or measuring a controlled substance;

2-12                       (F)  a dilutant [diluent] or adulterant, such as

2-13     quinine hydrochloride, mannitol, inositol, nicotinamide [mannite],

2-14     dextrose, [or] lactose, or absorbent, blotter-type material, that

2-15     is used or intended to be used to increase the amount or weight of

2-16     or to transfer [for use in cutting] a controlled substance

2-17     regardless of whether the dilutant or adulterant diminishes the

2-18     efficacy of the controlled substance;

2-19                       (G)  a separation gin or sifter used or intended

2-20     for use in removing twigs and seeds from or in otherwise cleaning

2-21     or refining marihuana;

2-22                       (H)  a blender, bowl, container, spoon, or mixing

2-23     device used or intended for use in compounding a controlled

2-24     substance;

2-25                       (I)  a capsule, balloon, envelope, or other

2-26     container used or intended for use in packaging small quantities of

2-27     a controlled substance;

2-28                       (J)  a container or other object used or intended

2-29     for use in storing or concealing a controlled substance;

2-30                       (K)  a hypodermic syringe, needle, or other

2-31     object used or intended for use in parenterally injecting a

2-32     controlled substance into the human body; and

2-33                       (L)  an object used or intended for use in

2-34     ingesting, inhaling, or otherwise introducing marihuana, cocaine,

2-35     hashish, or hashish oil into the  human body, including:

2-36                             (i)  a metal, wooden, acrylic, glass,

2-37     stone, plastic, or ceramic pipe with or without a screen, permanent

2-38     screen, hashish head, or punctured  metal bowl;

2-39                             (ii)  a water pipe;

2-40                             (iii)  a carburetion tube or device;

2-41                             (iv)  a smoking or carburetion mask;

2-42                             (v)  a chamber pipe;

2-43                             (vi)  a carburetor pipe;

2-44                             (vii)  an electric pipe;

2-45                             (viii)  an air-driven pipe;

2-46                             (ix)  a chillum;

2-47                             (x)  a bong; or

2-48                             (xi)  an ice pipe or chiller.

2-49                 (30)  "Opiate" means a substance that has an

2-50     addiction-forming or addiction-sustaining liability similar to

2-51     morphine or is capable of conversion  into a drug having

2-52     addiction-forming or addiction-sustaining liability.  The term

2-53     includes its racemic and levorotatory forms. The term does not

2-54     include, unless specifically designated as controlled under

2-55     Subchapter B [Section 481.038], the dextrorotatory isomer of

2-56     3-methoxy-n-methylmorphinan and its salts (dextromethorphan).

2-57                 (41)  "Prescription" means an order by a practitioner

2-58     to a pharmacist for a controlled substance for a particular patient

2-59     that specifies:

2-60                       (A)  the date of issue;

2-61                       (B)  the name and address of the patient or, if

2-62     the controlled substance is prescribed for an animal, the species

2-63     of the animal and the name and address of its owner;

2-64                       (C)  the name and quantity of the controlled

2-65     substance prescribed with the quantity shown numerically followed

2-66     by the number written as a word if the order is written or, if the

2-67     order is communicated orally or telephonically, with the quantity

2-68     given by the practitioner and transcribed by the pharmacist

2-69     numerically;

 3-1                       (D)  directions for the use of the drug; [and]

 3-2                       [(E)  the legibly printed or stamped name,

 3-3     address, Federal Drug Enforcement Administration registration

 3-4     number, and telephone number of the practitioner at the

 3-5     practitioner's usual place of business.]

 3-6                       (E)  the intended use of the drug unless the

 3-7     practitioner determines the furnishing of this information is not

 3-8     in the best interest of the patient; and

 3-9                       (F)  the legibly printed or stamped name,

3-10     address, Federal Drug Enforcement Administration registration

3-11     number, and telephone number of the practitioner at the

3-12     practitioner's usual place of business[, legibly printed or

3-13     stamped].

3-14                 (50)  "Abuse unit" means:

3-15                       (A)  except as provided by Paragraph (B):

3-16                             (i)  a single unit on or in any adulterant,

3-17     dilutant, or similar carrier medium, including marked or perforated

3-18     blotter paper, a tablet,  gelatin wafer, sugar cube, or stamp, or

3-19     other medium that contains any amount of a controlled substance

3-20     listed in Penalty Group 1-A, if the unit is commonly used in abuse

3-21     of that substance; or

3-22                             (ii)  each quarter-inch square section of

3-23     paper, if the adulterant, dilutant, or carrier medium is paper not

3-24     marked or perforated into  individual abuse units; or

3-25                       (B)  if the controlled substance is in liquid

3-26     form, 40 micrograms of the controlled substance including any

3-27     adulterant or dilutant.

3-28           SECTION 2.  Subchapter B, Chapter 481, Health and Safety

3-29     Code, is amended to read as follows:

3-30                          SUBCHAPTER B.  SCHEDULES

3-31           Sec. 481.031.  NOMENCLATURE.   Controlled substances listed

3-32     in Schedules I through V and Penalty Groups 1 through 4 are

3-33     included by whatever official,  common, usual, chemical, or trade

3-34     name they may be designated.

3-35           Sec. 481.032.  SCHEDULES.  (a) The commissioner shall

3-36     establish and modify the following schedules of controlled

3-37     substances under this subchapter:   Schedule I, Schedule I-A,

3-38     Schedule II, Schedule III, Schedule IV, and Schedule V.

3-39           (b)  A reference to a schedule in this chapter means the most

3-40     current version of the schedule established or altered by the

3-41     commissioner under this  subchapter and published in the Texas

3-42     Register on or after January 1, 1998. [SCHEDULE I.  (a) Schedule I

3-43     consists of:]

3-44                 [(1)  the following opiates,  including their isomers,

3-45     esters, ethers, salts, and salts of isomers, esters, and ethers,

3-46     unless specifically excepted, if the existence of these  isomers,

3-47     esters, ethers, and salts is possible within the specific chemical

3-48     designation:]

3-49                       [Alfentanil;]

3-50                       [Allylprodine;]

3-51                       [Alpha-methylfentanyl or another  derivative of

3-52     Fentanyl;]

3-53                       [Benzethidine;]

3-54                       [Betaprodine;]

3-55                       [Clonitazene;]

3-56                       [Diampromide;]

3-57                       [Diethylthiambutene;]

3-58                       [Difenoxin;]

3-59                       [Dimenoxadol;]

3-60                       [Dimethylthiambutene;]

3-61                       [Dioxaphetyl butyrate;]

3-62                       [Dipipanone;]

3-63                       [Ethylmethylthiambutene;]

3-64                       [Etonitazene;]

3-65                       [Etoxeridine;]

3-66                       [Furethidine;]

3-67                       [Hydroxypethidine;]

3-68                       [Ketobemidone;]

3-69                       [Levophenacylmorphan;]

 4-1                       [Meprodine;]

 4-2                       [Methadol;]

 4-3                       [Moramide;]

 4-4                       [Morpheridine;]

 4-5                       [Noracymethadol;]

 4-6                       [Norlevorphanol;]

 4-7                       [Normethadone;]

 4-8                       [Norpipanone;]

 4-9                       [Phenadoxone;]

4-10                       [Phenampromide;]

4-11                       [Phencyclidine;]

4-12                       [Phenomorphan;]

4-13                       [Phenoperidine;]

4-14                       [Piritramide;]

4-15                       [Proheptazine;]

4-16                       [Properidine;]

4-17                       [Propiram;]

4-18                       [Tilidine; and]

4-19                       [Trimeperidine;]

4-20                 [(2)  the following opium derivatives, their  salts,

4-21     isomers, and salts of isomers, unless specifically excepted, if the

4-22     existence of these salts, isomers, and salts of isomers is possible

4-23     within the specific chemical designation:]

4-24                       [Acetorphine;]

4-25                       [Acetyldihydrocodeine;]

4-26                       [Benzylmorphine;]

4-27                       [Codeine methylbromide;]

4-28                       [Codeine-N-Oxide;]

4-29                       [Cyprenorphine;]

4-30                       [Desomorphine;]

4-31                       [Dihydromorphine;]

4-32                       [Drotebanol;]

4-33                       [Etorphine (except hydrochloride salt);]

4-34                       [Heroin;]

4-35                       [Hydromorphinol;]

4-36                       [Methyldesorphine;]

4-37                       [Methyldihydromorphine;]

4-38                       [Monoacetylmorphine;]

4-39                       [Morphine methylbromide;]

4-40                       [Morphine methylsulfonate;]

4-41                       [Morphine-N-Oxide;]

4-42                       [Myrophine;]

4-43                       [Nicocodeine;]

4-44                       [Nicomorphine;]

4-45                       [Normorphine;]

4-46                       [Pholcodine; and]

4-47                       [Thebacon;]

4-48                 [(3)  unless specifically excepted or unless listed in

4-49     another schedule, a material, compound, mixture, or preparation

4-50     that contains any  quantity of the following hallucinogenic

4-51     substances or that contains any of the substance's salts, isomers,

4-52     and salts of isomers if the existence of  the salts, isomers, and

4-53     salts of isomers is possible within the specific chemical

4-54     designation:]

4-55                       [4-bromo-2, 5-dimethoxyamphetamine (some trade or

4-56     other  names:  4-bromo-2, 5-dimethoxy-alpha-methylphenethylamine;

4-57     4-bromo-2, 5-DMA);]

4-58                       [2, 5-dimethoxyamphetamine (some trade or other

4-59     names:  2,  5-dimethoxy-alpha-methylphenethylamine; 2, 5-DMA);]

4-60                       [5-methoxy-3, 4-methylenedioxy amphetamine;]

4-61                       [4-methoxyamphetamine (some trade or other names:

4-62     4-methoxy-alpha-methylphenethylamine; paramethoxyamphetamine; PMA);]

4-63                       [1-methyl-4-phenyl-1, 2, 5, 6-tetrahydro-pyridine

4-64     (MPTP);]

4-65                       [1-methyl-4-phenyl-4-propionoxy-piperidine (MPPP,

4-66     PPMP);]

4-67                       [4-methyl-2, 5-dimethoxyamphetamine (some trade

4-68     and other names:  4-methyl-2,

4-69     5-dimethoxy-alpha-methylphenethylamine; "DOM";  and "STP");]

 5-1                       [3, 4-methylene-dioxy methamphetamine (MDMA,

 5-2     MDM);]

 5-3                       [3, 4-methylenedioxy amphetamine;]

 5-4                       [3, 4,  5-trimethoxy amphetamine;]

 5-5                       [Bufotenine (some trade and other names:

 5-6     3-(beta-Dimethylaminoethyl)-5-hydroxyindole;

 5-7     3-(2-dimethylaminoethyl)-5-indolol; N, N-dimethylserotonin;

 5-8     5-hydroxy-N, N-dimethyltryptamine; mappine);]

 5-9                       [Diethyltryptamine (some trade and other names:

5-10     N, N-Diethyltryptamine, DET);]

5-11                       [Dimethyltryptamine (some trade and other names:

5-12     DMT);]

5-13                       [Ethylamine Analog of Phencyclidine (some trade

5-14     or other names: N-ethyl-1-phenylcyclohexylamine;

5-15     (1-phenylcyclohexyl) ethylamine; N-(1-phenylcyclohexyl) ethylamine,

5-16     cyclohexamine, PCE);]

5-17                       [Ibogaine (some trade or other names:  7-Ethyl-6,

5-18     6, beta, 7, 8, 9, 10, 12, 13,--octahydro-2-methoxy-6,

5-19     9-methano-5H-pyrido (1', 2':1, 2) azepino (5, 4-b) indole;

5-20     tabernanthe iboga);]

5-21                       [Lysergic acid diethylamide;]

5-22                       [Marihuana;]

5-23                       [Mescaline;]

5-24                       [N-ethyl-3-piperidyl benzilate;]

5-25                       [N-methyl-3-piperidyl benzilate;]

5-26                       [Parahexyl (some trade or other names:

5-27     3-Hexyl-1-hydroxy-7, 8, 9, 10-tetrahydro-6, 6,

5-28     9-tri-methyl-6H-dibenzo (b,d) pyran;  Synhexyl);]

5-29                       [Peyote, unless unharvested and growing in its

5-30     natural state, meaning all parts of the plant classified

5-31     botanically as Lophophora, whether growing or not, the seeds of the

5-32     plant, an extract from a part of the plant, and every compound,

5-33     manufacture, salt, derivative, mixture, or preparation of the

5-34     plant, its seeds, or extracts;]

5-35                       [Psilocybin;]

5-36                       [Psilocin;]

5-37                       [Pyrrolidine Analog of Phencyclidine (some trade

5-38     or other names:  1-(1-phenylcyclohexyl)-pyrrolidine, PCPy, PHP);]

5-39                       [Synthetic equivalents of the substances

5-40     contained in the plant Cannabis, or in the resinous extractives of

5-41     that plant, and synthetic substances, derivatives, and their

5-42     isomers with similar chemical structure and pharmacological

5-43     activity such as:]

5-44                       [delta-1 cis or trans tetrahydrocannabinol, and

5-45     their optical isomers;]

5-46                       [delta-6  cis or trans tetrahydrocannabinol, and

5-47     their optical isomers;]

5-48                       [delta-3, 4 cis or trans tetrahydrocannabinol,

5-49     and its optical isomers;]

5-50                       [(Compounds of  these structures, regardless of

5-51     numerical designation of atomic positions, since nomenclature of

5-52     these substances is not internationally  standardized);]

5-53                       [Tetrahydrocannabinols; and]

5-54                       [Thiophene Analog of Phencyclidine (some trade or

5-55     other names:  1-(1-(2-thienyl) cyclohexyl) piperidine;  2-Thienyl

5-56     Analog of Phencyclidine; TPCP);]

5-57                 [(4)  unless specifically excepted or unless listed in

5-58     another schedule, a material, compound, mixture, or  preparation

5-59     that contains any quantity of the following substances having a

5-60     depressant or stimulant effect on the central nervous system,

5-61     including  the substance's salts, isomers, and salts of isomers if

5-62     the existence of the salts, isomers, and salts of isomers is

5-63     possible within the specific chemical designation:]

5-64                       [Fenethylline;]

5-65                       [Mecloqualone;]

5-66                       [Methaqualone;]

5-67                       [N-ethylamphetamine; and]

5-68                       [Nitrazepam; and]

5-69                 [(5)  temporary listing of substances subject to

 6-1     emergency scheduling by the Federal Drug Enforcement

 6-2     Administration, and any material, compound, mixture, or preparation

 6-3     that contains any quantity  of the following substances:]

 6-4                       [N, N-dimethylamphetamine (Some trade or other

 6-5     names:  N,N,alpha-trimethylbenzeneethaneamine;

 6-6     N,N,alpha-trimethylphenethylamine; including its salts, optical

 6-7     isomers, and salts of optical isomers);]

 6-8                       [4-methylaminorex;]

 6-9                       [3, 4-methylenedioxy  N-ethylamphetamine (Also

6-10     known as N-ethyl MDA);]

6-11                       [N-hydroxy-3,4-methylenedioxyamphetamine (Also

6-12     known as N-hydroxy MDA).]

6-13           [(b)  For the purposes of  Subsection (a)(3) only, the term

6-14     "isomer" includes optical, position, and geometric isomers.]

6-15           [Sec. 481.033.  SCHEDULE II.  Schedule II consists of:]

6-16                         [(1)  the following substances, however

6-17     produced, except those narcotic drugs listed in other schedules:]

6-18                       [(A)  Opium and opiate, and a salt, compound,

6-19     derivative, or preparation of opium or opiate, other than naloxone

6-20     and its salts and naltrexone and its salts, but including:]

6-21                             [Codeine;]

6-22                             [Ethylmorphine;]

6-23                             [Etorphine hydrochloride;]

6-24                             [Granulated opium;]

6-25                             [Hydrocodone;]

6-26                             [Hydromorphone;]

6-27                             [Metopon;]

6-28                             [Morphine;]

6-29                             [Opium extracts;]

6-30                             [Opium fluid extracts;]

6-31                             [Oxycodone;]

6-32                             [Oxymorphone;]

6-33                             [Powdered opium;]

6-34                             [Raw opium;]

6-35                             [Thebaine; and]

6-36                             [Tincture of opium;]

6-37                       [(B)  a salt, compound, isomer, derivative, or

6-38     preparation of a substance that  is chemically equivalent or

6-39     identical to a substance described by Paragraph (A), other than the

6-40     isoquinoline alkaloids of opium;]

6-41                       [(C)  Opium poppy and  poppy straw;]

6-42                       [(D)  Cocaine, including:]

6-43                             [(i)  its salts, its optical, position, and

6-44     geometric isomers, and the salts of those isomers; and]

6-45                             [(ii)  coca leaves  and a salt, compound,

6-46     derivative, or preparation of coca leaves that is chemically

6-47     equivalent or identical to a substance described by this

6-48     subparagraph or Subparagraph (i), other than decocainized coca

6-49     leaves or extractions of coca leaves that do not contain cocaine or

6-50     ecgonine; and]

6-51                       [(E)  Concentrate of poppy straw, meaning the

6-52     crude extract of poppy straw in liquid, solid, or powder form that

6-53     contains the phenanthrine alkaloids of the  opium poppy;]

6-54                 [(2)  the following opiates, including their isomers,

6-55     esters, ethers, salts, and salts of isomers, if the existence of

6-56     these isomers,  esters, ethers, and salts is possible within the

6-57     specific chemical designation:]

6-58                       [Alphaprodine;]

6-59                       [Anileridine;]

6-60                       [Bezitramide;]

6-61                       [Dextropropoxyphene, bulk  (nondosage form);]

6-62                       [Dihydrocodeine;]

6-63                       [Diphenoxylate;]

6-64                       [Fentanyl;]

6-65                       [Isomethadone;]

6-66                       [Levomethorphan;]

6-67                       [Levorphanol;]

6-68                       [Metazocine;]

6-69                       [Methadone;]

 7-1                       [Methadone-Intermediate,

 7-2     4-cyano-2-dimethylamino-4, 4-diphenyl butane;]

 7-3                       [Moramide-Intermediate, 2-methyl-3-morpholino-1,

 7-4     1-diphenyl-propane-carboxylic acid;]

 7-5                       [Pethidine;]

 7-6                       [Pethidine-Intermediate-A,

 7-7     4-cyano-1-methyl-4-phenylpiperidine;]

 7-8                       [Pethidine-Intermediate-B,

 7-9     ethyl-4-phenylpiperidine-4-carboxylate;]

7-10                       [Pethidine-Intermediate-C,

7-11     1-methyl-4-phenylpiperidine-4-carboxylic acid;]

7-12                       [Phenazocine;]

7-13                       [Piminodine;]

7-14                       [Racemethorphan;]

7-15                       [Racemorphan; and]

7-16                       [Sufentanil;]

7-17                 [(3)  unless listed in another schedule and except as

7-18     provided by Section 481.037, a material, compound, mixture, or

7-19     preparation that contains any quantity of the following substances

7-20     having a potential for abuse associated with a stimulant effect on

7-21     the central  nervous system:]

7-22                       [Amphetamine, its salts, optical isomers, and

7-23     salts of its optical isomers;]

7-24                       [Methamphetamine, including its salts, optical

7-25     isomers, and  salts of optical isomers;]

7-26                       [Methylphenidate and its salts; and]

7-27                       [Phenmetrazine and its salts;]

7-28                 [(4)  unless listed in another schedule, a material,

7-29     compound, mixture, or preparation that contains any quantity of the

7-30     following substances having a depressant effect on the central

7-31     nervous system,  including the substance's salts, isomers, and

7-32     salts of isomers if the existence of the salts, isomers, and salts

7-33     of isomers is possible within the  specific chemical designation:]

7-34                       [Amobarbital;]

7-35                       [Secobarbital; and]

7-36                       [Pentobarbital;]

7-37                 [(5)  unless specifically excepted or listed in another

7-38     schedule, a  material, compound, mixture, or preparation that

7-39     contains any quantity of the following substances:]

7-40                       [Immediate precursor to methamphetamine:]

7-41                       [Phenylacetone and methylamine if possessed

7-42     together with intent to manufacture methamphetamine;]

7-43                       [Immediate precursor to amphetamine and

7-44     methamphetamine:]

7-45                       [Phenylacetone (some trade or other names:

7-46     phenyl-2-propanone;  P2P; benzyl methyl ketone; methyl benzyl

7-47     ketone); and]

7-48                       [Immediate  precursors to phencyclidine (PCP):]

7-49                       [1-phenylcyclohexylamine; and]

7-50                       [1-piperidinocyclohexanecarbonitrile (PCC).]

7-51           [Sec. 481.034.  SCHEDULE III.  Schedule III  consists of:]

7-52                 [(1) unless listed in another schedule and except as

7-53     provided by Section 481.037, a material, compound, mixture, or

7-54     preparation that  contains any quantity of the following substances

7-55     having a potential for abuse associated with a depressant effect on

7-56     the central nervous system:]

7-57                       [a  compound, mixture, or preparation containing

7-58     amobarbital, secobarbital, pentobarbital, or any of their salts and

7-59     one or more active medicinal  ingredients that are not listed in a

7-60     schedule;]

7-61                       [a suppository dosage form containing

7-62     amobarbital, secobarbital, pentobarbital, or any of their salts

7-63     and approved by the Food and Drug Administration for marketing only

7-64     as a suppository;]

7-65                       [a substance that contains any quantity of a

7-66     derivative of  barbituric  acid, or any salt of a derivative of

7-67     barbituric acid, except those substances that are specifically

7-68     listed in other schedules;]

7-69                             [Chlorhexadol;]

 8-1                             [Glutethimide;]

 8-2                             [Lysergic acid;]

 8-3                             [Lysergic acid amide;]

 8-4                             [Methyprylon;]

 8-5                             [Sulfondiethylmethane;]

 8-6                             [Sulfonethylmethane; and]

 8-7                             [Sulfonmethane;]

 8-8                 [(2)  Nalorphine;]

 8-9                 [(3)  a material, compound, mixture, or preparation

8-10     containing limited quantities of any of the following narcotic

8-11     drugs, or any of their  salts:]

8-12                       [not more than 1.8 grams of codeine, or any of

8-13     its salts, per 100 milliliters or not more than 90 milligrams per

8-14     dosage unit, with an equal or  greater quantity of an isoquinoline

8-15     alkaloid of opium;]

8-16                       [not more than 1.8 grams of codeine, or any of

8-17     its salts, per 100 milliliters or not more than  90 milligrams per

8-18     dosage unit, with one or more active, nonnarcotic ingredients in

8-19     recognized therapeutic amounts;]

8-20                       [not more than 300 milligrams of

8-21     dihydrocodeinone, or any of its salts, per 100 milliliters or not

8-22     more than 15 milligrams per dosage unit, with a fourfold or greater

8-23     quantity of an  isoquinoline alkaloid of opium;]

8-24                       [not more than 300 milligrams of

8-25     dihydrocodeinone, or any of its salts, per 100 milliliters or not

8-26     more than 15 milligrams per dosage unit, with one or more active,

8-27     nonnarcotic ingredients in recognized therapeutic amounts;]

8-28                       [not more than 1.8 grams of  dihydrocodeine, or

8-29     any of its salts, per 100 milliliters or not more than 90

8-30     milligrams per dosage unit, with one or more active, nonnarcotic

8-31     ingredients in recognized therapeutic amounts;]

8-32                       [not more than 300 milligrams of ethylmorphine,

8-33     or any of its salts, per 100 milliliters or not more  than 15

8-34     milligrams per dosage unit, with one or more ingredients in

8-35     recognized therapeutic amounts;]

8-36                       [not more than 500 milligrams of opium per 100

8-37     milliliters or per 100 grams, or not more than 25 milligrams per

8-38     dosage unit, with one or more active, nonnarcotic ingredients in

8-39     recognized  therapeutic amounts;]

8-40                       [not more than 50 milligrams of morphine, or any

8-41     of its salts, per 100 milliliters or per 100 grams with one or more

8-42     active,  nonnarcotic ingredients in recognized therapeutic amounts;

8-43     and]

8-44                 [(4)  unless listed in another schedule, a material,

8-45     compound, mixture, or preparation  that contains any quantity of

8-46     the following substances having a stimulant effect on the central

8-47     nervous system, including the substance's salts,  optical,

8-48     position, or geometric isomers, and salts of the substance's

8-49     isomers, if the existence of the salts, isomers, and salts of

8-50     isomers is  possible within the specific chemical designation:]

8-51                       [Benzphetamine;]

8-52                       [Chlorphentermine;]

8-53                       [Clortermine; and]

8-54                       [Phendimetrazine.]

8-55           [Sec. 481.035.  SCHEDULE IV.  Schedule IV consists of:]

8-56                 [(1)  except as provided by Section 481.037, a

8-57     material, compound, mixture, or preparation that contains any

8-58     quantity of the  following substances having a potential for abuse

8-59     associated with a depressant effect on the central nervous system:]

8-60                       [Alprazolam;]

8-61                       [Barbital;]

8-62                       [Chloral  betaine;]

8-63                       [Chloral hydrate;]

8-64                       [Chlordiazepoxide;]

8-65                       [Clonazepam;]

8-66                       [Clorazepate;]

8-67                       [Diazepam;]

8-68                       [Ethchlorvynol;]

8-69                       [Ethinamate;]

 9-1                       [Flurazepam;]

 9-2                       [Halazepam;]

 9-3                       [Lorazepam;]

 9-4                       [Mebutamate;]

 9-5                       [Meprobamate;]

 9-6                       [Methohexital;]

 9-7                       [Methylphenobarbital;]

 9-8                       [Oxazepam;]

 9-9                       [Paraldehyde;]

9-10                       [Pentazocine, its salts, derivatives, compounds,

9-11     or mixtures;]

9-12                       [Petrichloral;]

9-13                       [Phenobarbital;]

9-14                       [Prazepam;]

9-15                       [Temazepam; and]

9-16                       [Triazolam;]

9-17                 [(2)  unless listed in another schedule, a material,

9-18     compound, mixture, or preparation that contains any quantity of the

9-19     following substances having a stimulant effect on the central

9-20     nervous system, including the substance's salts, optical, position,

9-21     or geometric isomers, and salts of those isomers if the existence

9-22     of the salts, isomers, and salts of isomers is possible within the

9-23     specific  designation:]

9-24                       [Diethylpropion;]

9-25                       [Fenfluramine;]

9-26                       [Mazindol;]

9-27                       [Pemoline (including organometallic complexes and

9-28     their chelates);]

9-29                       [Phentermine;]

9-30                       [Pipradol; and]

9-31                       [SPA ((-)-1-dimethyamino-1, 2-diphenylethane);]

9-32                 [(3)  unless specifically excepted or unless listed in

9-33     another schedule, a material, compound, mixture, or  preparation

9-34     that contains any quantity of the following substances, including

9-35     the substance's salts:]

9-36                       [Dextropropoxyphene (Alpha-(+)-4-dimethylamino-1,

9-37     2-diphenyl-3-methyl-2-propionoxybutane);]

9-38                 [(4)  unless specifically excepted or unless listed in

9-39     another schedule, a material, compound, mixture, or  preparation

9-40     containing limited quantities of the following narcotic drug or its

9-41     salts:]

9-42                       [not more than 1 milligram of difenoxin and not

9-43     less than 25  micrograms of atropine sulfate per dosage unit; and]

9-44                 [(5)  any human growth hormone or any of the following

9-45     anabolic steroids, or any isomer, ester,  salt, or derivative of

9-46     the following that acts in the same manner on the human body:]

9-47                       [Clostebol;]

9-48                       [Dehydrochlormethyltestosterone;]

9-49                       [Ethylestrenol;]

9-50                       [Fluoxymesterone;]

9-51                       [Mesterolone;]

9-52                       [Methandienone;]

9-53                       [Methandrostenolone;]

9-54                       [Methenolone;]

9-55                       [Methyltestosterone;]

9-56                       [Nandrolone;]

9-57                       [Norethandrolone;]

9-58                       [Oxandrolone;]

9-59                       [Oxymesterone;]

9-60                       [Oxymetholone;]

9-61                       [Stanozolol; and]

9-62                       [Testosterone.]

9-63           [Sec. 481.036.  SCHEDULE V.  Schedule V consists of a

9-64     controlled substance that is a  compound, mixture, or preparation

9-65     containing limited quantities of any of the following narcotic

9-66     drugs that also contain one or more nonnarcotic  active medicinal

9-67     ingredients in sufficient proportion to confer on the compound,

9-68     mixture, or preparation valuable medicinal qualities other than

9-69     those  possessed by the narcotic drug alone:]

 10-1                [(1)  not more than 200 milligrams of codeine, or any

 10-2    of its salts, per 100 milliliters or per 100 grams;]

 10-3                [(2)  not  more than 100 milligrams of dihydrocodeine,

 10-4    or any of its salts, per 100 milliliters or per 100 grams;]

 10-5                [(3)  not more than 100 milligrams of  ethylmorphine,

 10-6    or any of its salts, per 100 milliliters or per 100 grams;]

 10-7                [(4)  not more than 2.5 milligrams of diphenoxylate and

 10-8    not less  than 25  micrograms of atropine sulfate per dosage unit;]

 10-9                [(5)  not more than 15 milligrams of opium per 29.5729

10-10    milliliters or per 28.35 grams; and]

10-11                [(6)  not more than 0.5 milligrams of difenoxin and not

10-12    less than 25 micrograms of atropine sulfate per dosage unit.]

10-13          Sec. 481.033 [481.037].  EXCLUSION FROM SCHEDULES AND

10-14    APPLICATION OF ACT.  (a)  A nonnarcotic substance is excluded from

10-15    Schedules I  through V if the substance may lawfully be sold over

10-16    the counter without a prescription, under the Federal Food, Drug,

10-17    and Cosmetic Act (21 U.S.C.  Section 301 et seq.).

10-18          (b)  The commissioner may not include in the schedules:

10-19                (1)  a substance described by Subsection (a); or

10-20                (2)  distilled spirits, wine, malt beverages, or

10-21    tobacco.

10-22          (c)  A compound, mixture, or preparation containing a

10-23    stimulant substance listed in Schedule II and having a potential

10-24    for abuse associated with a stimulant effect on the central nervous

10-25    system [Section 481.033(3)] is excepted from the  application of

10-26    this chapter if the compound, mixture, or preparation contains one

10-27    or more active medicinal ingredients not having a stimulant effect

10-28    on the central nervous system and if the admixtures are included in

10-29    combinations, quantity, proportions, or concentrations that vitiate

10-30    the potential  for abuse of the substance having a stimulant effect

10-31    on the central nervous system.

10-32          (d)  A compound, mixture, or preparation containing a

10-33    depressant substance listed in Schedule III or IV and having a

10-34    potential for abuse associated with a depressant effect on the

10-35    central nervous system [Section 481.034(1) or 481.035(1)] is

10-36    excepted from the application of this chapter if the compound,

10-37    mixture, or preparation contains one or more active medicinal

10-38    ingredients not  having a depressant effect on the central nervous

10-39    system and if the admixtures are included in combinations,

10-40    quantity, proportions, or concentrations  that vitiate the

10-41    potential for abuse of the substance having a depressant effect on

10-42    the central nervous system.

10-43          (e)  A nonnarcotic prescription substance is exempted from

10-44    Schedules I through V and the application of this chapter to the

10-45    same extent that the  substance has been exempted from the

10-46    application of the Federal Controlled Substances Act, if the

10-47    substance is listed as an exempt prescription  product under 21

10-48    C.F.R. Section 1308.32 and its subsequent amendments.

10-49          (f)  A chemical substance that is intended for laboratory,

10-50    industrial, educational, or special research purposes and not for

10-51    general administration to a human being or other animal is exempted

10-52    from Schedules I through V and the application of this chapter to

10-53    the same extent that the substance has  been exempted from the

10-54    application of the Federal Controlled Substances Act, if the

10-55    substance is listed as an exempt chemical preparation under 21

10-56    C.F.R. Section 1308.24 and its subsequent amendments.

10-57          (g)  An anabolic steroid product, which has no significant

10-58    potential for abuse due to concentration, preparation, mixture, or

10-59    delivery system, is  exempted from Schedules I through V and the

10-60    application of this chapter to the same extent that the substance

10-61    has been exempted from the application  of the Federal Controlled

10-62    Substances Act, if the substance is listed as an exempt anabolic

10-63    steroid product under 21 C.F.R. Section 1308.34 and its  subsequent

10-64    amendments.

10-65          Sec. 481.034 [481.038].  ESTABLISHMENT AND MODIFICATION

10-66    [ALTERATION] OF SCHEDULES BY COMMISSIONER.  (a)  The commissioner

10-67    shall establish schedules of controlled [, with the approval of the

10-68    Texas Board of Health, may add] substances as described by Section

10-69    481.032 [to Schedules I through V] and may add, delete, or

 11-1    reschedule substances listed in those schedules.  The commissioner

 11-2    shall assign a controlled substance to a schedule:

 11-3                (1)  in accordance with [subject to] Section 481.035;

 11-4    and

 11-5                (2)  in a manner consistent with this subchapter

 11-6    [481.039].

 11-7          (b)  Except for alterations in schedules required by

 11-8    Subsection (g), the commissioner may not make an alteration in a

 11-9    schedule unless the commissioner  holds a public hearing on the

11-10    matter in Austin.

11-11          (c)  The commissioner may not:

11-12                (1)  add a substance to the schedules if[:]

11-13                [(1)]  the substance has been deleted from the

11-14    schedules by the legislature; [or]

11-15                (2)  delete a substance from the schedules if the

11-16    substance has been added to the schedules by the legislature; or

11-17                (3)  reschedule a substance if the substance has been

11-18    placed in a schedule by the legislature [legislation attempting to

11-19    add the  substance to the schedules has failed to pass when

11-20    considered by a quorum of either house of the legislature].

11-21          (d)  In making a determination regarding a substance, the

11-22    commissioner shall consider:

11-23                (1)  the actual or relative potential for its abuse;

11-24                (2)  the scientific evidence of its pharmacological

11-25    effect, if known;

11-26                (3)  the state of current scientific knowledge

11-27    regarding the substance;

11-28                (4)  the history and current pattern of its abuse;

11-29                (5)  the scope, duration, and significance of its

11-30    abuse;

11-31                (6)  the risk to the public health;

11-32                (7)  the potential of the substance to produce

11-33    psychological or physiological dependence liability; and

11-34                (8)  whether the substance is an immediate precursor of

11-35    a substance already controlled under this chapter.

11-36          (e)  After considering the factors listed in Subsection (d),

11-37    the commissioner shall make findings with respect to those factors

11-38    and adopt a rule  controlling the substance if the commissioner

11-39    finds the substance has a potential for abuse.

11-40          (f)  If the commissioner designates a substance as an

11-41    immediate precursor, a substance that is a precursor of the

11-42    controlled precursor is not subject  to control solely because it

11-43    is a precursor of the controlled precursor.

11-44          (g)  Except as otherwise provided by this subsection, if a

11-45    substance is designated, rescheduled, or deleted as a controlled

11-46    substance  under federal law and notice of that fact is given to

11-47    the commissioner, the commissioner similarly shall control the

11-48    substance under this chapter.  After the expiration of a 30-day

11-49    period beginning on the day after the date of publication in the

11-50    Federal Register of a final order designating a  substance as a

11-51    controlled substance or rescheduling or deleting a substance, the

11-52    commissioner similarly shall designate, reschedule, or delete the

11-53    substance, unless the commissioner objects during the period. If

11-54    the commissioner objects, the commissioner shall  publish the

11-55    reasons for the objection and give all interested parties an

11-56    opportunity to be heard. At the conclusion of the hearing, the

11-57    commissioner  shall publish a decision, which is final unless

11-58    altered by statute. On publication of an objection by the

11-59    commissioner, control as to that particular  substance under this

11-60    chapter is stayed until the commissioner publishes the

11-61    commissioner's decision.

11-62          (h)  Not later than the 10th day after the date on which the

11-63    commissioner designates [adds], deletes, or reschedules a substance

11-64    under Subsection (a), the commissioner shall give written notice of

11-65    that action to the director and to each state licensing agency

11-66    having jurisdiction over practitioners.

11-67          Sec. 481.035 [481.039].  FINDINGS.  (a)  The commissioner

11-68    shall place a substance in Schedule I if the commissioner finds

11-69    that the  substance:

 12-1                (1)  has a high potential for abuse; and

 12-2                (2)  has no accepted medical use in treatment in the

 12-3    United States or lacks accepted safety for use in treatment under

 12-4    medical supervision.

 12-5          (b)  The commissioner shall place a substance in Schedule II

 12-6    if the commissioner finds that:

 12-7                (1)  the substance has a high potential for abuse;

 12-8                (2)  the substance has currently accepted medical use

 12-9    in treatment in the United States; and

12-10                (3)  abuse of the substance may lead to severe

12-11    psychological or physical dependence.

12-12          (c)  The commissioner shall place a substance in Schedule III

12-13    if the commissioner finds that:

12-14                (1)  the substance has a potential for abuse less than

12-15    that of the substances listed in Schedules I and II;

12-16                (2)  the substance has currently accepted medical use

12-17    in treatment in the United States; and

12-18                (3)  abuse of the substance may lead to moderate or low

12-19    physical dependence or high psychological dependence.

12-20          (d)  The commissioner shall place a substance in Schedule IV

12-21    if the commissioner finds that:

12-22                (1)  the substance has a lower potential for abuse than

12-23    that of the substances listed in Schedule III;

12-24                (2)  the substance has currently accepted medical use

12-25    in treatment in the United States; and

12-26                (3)  abuse of the substance may lead to a more limited

12-27    physical or psychological dependence than that of the substances

12-28    listed in Schedule III.

12-29          (e)  The commissioner shall place a substance in Schedule V

12-30    if the commissioner finds that the substance:

12-31                (1)  has a lower potential for abuse than that of the

12-32    substances listed in Schedule IV;

12-33                (2)  has currently accepted medical use in treatment in

12-34    the United States; and

12-35                (3)  may lead to a more limited physical or

12-36    psychological dependence liability than that of the substances

12-37    listed in Schedule IV.

12-38          Sec. 481.036 [481.040].  PUBLICATION OF SCHEDULES.  (a)  The

12-39    commissioner shall publish the schedules [annually] by filing a

12-40    certified copy of the schedules with the secretary of state for

12-41    publication in the Texas Register not later than the fifth working

12-42    day after the date the commissioner takes action under this

12-43    subchapter.

12-44          (b)  Each published schedule must show changes, if any, made

12-45    in the schedule since its latest publication.

12-46          (c)  An action by the commissioner that establishes or

12-47    modifies a schedule under this subchapter may take effect not

12-48    earlier than the 21st day after the date on which the schedule or

12-49    modification is published in the Texas Register unless an

12-50    emergency exists that necessitates earlier action to avoid an

12-51    imminent hazard to the public safety.

12-52          SECTION 3.  Section 481.061(a), Health and Safety Code, is

12-53    amended to read as follows:

12-54          (a)  Except as otherwise provided by this chapter, a [A]

12-55    person who is not a registrant may not manufacture, distribute,

12-56    prescribe, possess, analyze, or dispense a controlled substance in

12-57    this state [without a registration issued under this subchapter].

12-58          SECTION 4.  Section 481.062(a), Health and Safety Code, is

12-59    amended to read as follows:

12-60          (a)  The following persons are not required to register and

12-61    may possess a controlled substance under this chapter:

12-62                (1)  an agent or employee of a registered manufacturer,

12-63    distributor, analyzer, or dispenser of the controlled substance

12-64    acting in the usual course  of business or employment;

12-65                (2)  a common or contract carrier, a warehouseman, or

12-66    an employee of a carrier or warehouseman whose possession of the

12-67    controlled substance is in  the usual course of business or

12-68    employment;

12-69                (3)  an ultimate user or a person in possession of the

 13-1    controlled substance under a lawful order of a practitioner or in

 13-2    lawful possession of the  controlled substance if it is listed in

 13-3    Schedule V;

 13-4                (4)  an officer or employee of this state, another

 13-5    state, or the United States who is lawfully engaged in the

 13-6    enforcement of a law relating to a controlled substance or drug or

 13-7    to a customs law and authorized to possess the controlled substance

 13-8    in the  discharge of the person's official duties; or

 13-9                (5) [(4)]  if the substance is tetrahydrocannabinol or

13-10    one of its derivatives:

13-11                      (A)  a Texas Department of Health official, a

13-12    medical school researcher, or a research program participant

13-13    possessing the substance as authorized under Subchapter G; or

13-14                      (B)  a practitioner or an ultimate user

13-15    possessing the substance as a participant in a federally approved

13-16    therapeutic research program that the  commissioner has reviewed

13-17    and found, in writing, to contain a medically responsible research

13-18    protocol.

13-19          SECTION 5.  Sections 481.0621(a) and (c), Health and Safety

13-20    Code, are amended to read as follows:

13-21          (a)  This subchapter does not apply to an educational or

13-22    research program of [a private school,] a school district[,] or a

13-23    public or private institution of higher education.  This subchapter

13-24    does not apply to a manufacturer, wholesaler, retailer, or other

13-25    person who sells, transfers, or furnishes materials covered by this

13-26    subchapter to those educational or research programs.

13-27          (c)  The department and the Texas [Central] Education Agency

13-28    shall adopt a memorandum of understanding that establishes the

13-29    responsibilities of the agency, the department, [private schools,]

13-30    and school districts in implementing and maintaining a program for

13-31    reporting information concerning controlled substances, controlled

13-32    substance analogues, chemical precursors, and chemical laboratory

13-33    apparatus used in educational or research activities of those

13-34    schools and school districts.

13-35          SECTION 6.  Sections 481.063(a), (e), (f), and (g), Health

13-36    and Safety Code, are amended to read as follows:

13-37          (a)  The director may refuse to [not] issue a registration to

13-38    a person to manufacture, distribute, analyze, or conduct research

13-39    with a controlled substance if the person fails or refuses to

13-40    provide to [unless] the director [receives] a consent form signed

13-41    by the person granting the director the right to inspect the

13-42    person's controlled premises and any record, controlled substance,

13-43    or other item covered by this chapter.

13-44          (e)  An application for registration to manufacture,

13-45    distribute, analyze, [or] dispense, or conduct research with a

13-46    controlled substance may be denied on a finding that the applicant:

13-47                (1)  has furnished [false or fraudulent] material

13-48    information in an application filed under this chapter that the

13-49    applicant knows is false or fraudulent;

13-50                (2)  has been convicted of or placed on community

13-51    supervision or other probation for:

13-52                      (A)  a felony;

13-53                      (B)  a violation of this chapter or of Chapters

13-54    482-485; or

13-55                      (C)  an offense reasonably related to the

13-56    registration sought;

13-57                (3)  has voluntarily surrendered or has had suspended,

13-58    denied, or revoked a registration or application for registration

13-59    to manufacture, distribute, analyze, or dispense controlled

13-60    substances under the Federal Controlled Substances Act;

13-61                (4)  has had suspended, probated, or revoked a

13-62    registration or a practitioner's license under the laws of this

13-63    state or another state;

13-64                (5)  has intentionally or knowingly failed to establish

13-65    and maintain effective security controls against diversion of

13-66    controlled substances into other than legitimate medical,

13-67    scientific, or industrial channels as provided by federal

13-68    regulations or laws, this chapter, or a rule adopted under this

13-69    chapter;

 14-1                (6)  has intentionally or knowingly [wilfully] failed

 14-2    to maintain records required to be kept by this chapter or a rule

 14-3    adopted  under this chapter;

 14-4                (7)  [or] has [wilfully or unreasonably] refused to

 14-5    allow an inspection authorized by this chapter or a rule adopted

 14-6    under this chapter; [or]

 14-7                (8) [(7)]  has intentionally or knowingly violated this

 14-8    chapter or a rule adopted under this chapter; or

 14-9                (9)  has voluntarily surrendered a registration that

14-10    has not been reinstated.

14-11          (f)  The director may inspect the premises or establishment

14-12    of an applicant for registration in accordance with this chapter.

14-13          (g)  A registration is valid until the first anniversary of

14-14    the date of issuance and may [must] be renewed [obtained] annually

14-15    under rules adopted by the director, unless a rule provides for a

14-16    longer period of validity or renewal.

14-17          SECTION 7.  Section 481.066, Health and Safety Code, is

14-18    amended to read as follows:

14-19          Sec. 481.066.  VOLUNTARY SURRENDER, CANCELLATION, SUSPENSION,

14-20    PROBATION, OR REVOCATION OF REGISTRATION.  (a)  The director [A

14-21    district court] may accept a voluntary surrender of a registration.

14-22          (b)  The director may cancel, suspend, or revoke a

14-23    registration, place on probation a person whose license has been

14-24    suspended, or reprimand a registrant for a cause described by

14-25    Section 481.063(e).

14-26          (c)  The director may cancel a registration that was issued

14-27    in error.

14-28          (d)  The director [The attorney representing the state in

14-29    district court or the attorney general shall file and prosecute

14-30    appropriate judicial proceedings for the suspension or revocation

14-31    of a registrant's registration on presentation of competent

14-32    evidence by the director.  A proceeding under this section may be

14-33    maintained in:]

14-34                [(1)  the registrant's county of residence;]

14-35                [(2)  the county in which the registrant maintains a

14-36    place of business or practice;]

14-37                [(3)  the county in which a wrongful act under Section

14-38    481.063(e) was committed; or]

14-39                [(4)  Travis County.]

14-40          [(b)  A petition for the suspension or revocation of a

14-41    registration is sufficient if it substantially complies with the

14-42    following requirements:]

14-43                [(1)  the petitioner must be "The State of Texas";]

14-44                [(2)  the petition must be directed to the registrant

14-45    whose license is sought to be suspended or revoked;]

14-46                [(3)  the petition must contain a short statement of

14-47    the cause of action sufficient to give notice of the grounds on

14-48    which suspension or revocation of the registration is sought;]

14-49                [(4)  the petition must ask for a suspension or

14-50    revocation of the registration; and]

14-51                [(5)  the petition must be verified by the director.]

14-52          [(c)  A court that suspends or revokes a registration] may

14-53    limit the cancellation, suspension, probation, or revocation to the

14-54    particular schedule or controlled substance within a schedule for

14-55    which grounds for cancellation, suspension, probation, or

14-56    revocation exist.

14-57          (e)  After accepting the voluntary surrender of a

14-58    registration or ordering the cancellation, suspension, probation,

14-59    or revocation of a registration, the director may seize or [(d)  If

14-60    a registration is suspended or revoked, at the time of suspension

14-61    or the effective date of the revocation order the court  may] place

14-62    under seal all controlled substances owned or possessed by the

14-63    registrant under the authority of that registration.  If the

14-64    director orders the cancellation, suspension, probation, or

14-65    revocation of a registration, a [A] disposition may not be made of

14-66    the seized or sealed substances [under seal] until the time for

14-67    administrative appeal of the order has elapsed or until all appeals

14-68    have been concluded, except that the director [on an application

14-69    the court] may order the sale of perishable substances and deposit

 15-1    of the proceeds of the sale in a special interest-bearing account

 15-2    in the general revenue fund [with the court].  When a surrender or

 15-3    cancellation, suspension, probation, or revocation order becomes

 15-4    final, all controlled substances may be forfeited to the state as

 15-5    provided under Subchapter E [Section 481.157].

 15-6          (f) [(e)]  The operation of a registrant in violation of this

 15-7    section is a public nuisance, and the director may apply to any

 15-8    court of competent jurisdiction for an injunction suspending the

 15-9    registration of the registrant.

15-10          (g)  Chapter 2001, Government Code, applies to a proceeding

15-11    [(f)  The Rules of Civil Procedure govern proceedings] under this

15-12    section to the extent that that chapter does [they do] not conflict

15-13    with this subchapter [section].

15-14          (h) [(g)]  The director shall promptly notify appropriate

15-15    state agencies of an order accepting a voluntary surrender or

15-16    canceling, suspending, probating, or revoking a registration and

15-17    the forfeiture of controlled substances.

15-18          (i)  The director shall give written notice to the applicant

15-19    or registrant of the acceptance of a voluntary surrender of a

15-20    registration, or of the cancellation, suspension, probation,

15-21    revocation, or denial of a registration.  The notice shall be sent

15-22    by registered mail, return receipt requested, to the most current

15-23    address of the applicant or registrant contained in the files of

15-24    the Department of Public Safety.

15-25          (j)  After a voluntary surrender, cancellation, suspension,

15-26    probation, revocation, or denial of a registration, on petition of

15-27    the applicant or former registrant, the director may issue or

15-28    reinstate the registration for good cause shown by the petitioner.

15-29          SECTION 8.  Sections 481.071(b) and (c), Health and Safety

15-30    Code, are amended to read as follows:

15-31          (b)  An anabolic steroid or human growth hormone listed in

15-32    Schedule III [Section 481.035] may only be:

15-33                (1)  dispensed, prescribed, delivered, or administered

15-34    by a practitioner, as defined by Section 481.002(39)(A), for a

15-35    valid medical purpose and in  the course of professional practice;

15-36    or

15-37                (2)  dispensed or delivered by a pharmacist according

15-38    to a prescription issued by a practitioner, as defined by Section

15-39    481.002(39)(A) or (C), for a  valid medical purpose and in the

15-40    course of professional practice.

15-41          (c)  For the purposes of Subsection (b), bodybuilding, muscle

15-42    enhancement, or increasing muscle bulk or strength through the use

15-43    of an anabolic steroid or human growth hormone listed in Schedule

15-44    III [Section 481.035] by a person who is in good health is not a

15-45    valid medical purpose.

15-46          SECTION 9.  Sections 481.074(h), (i), and (k), Health and

15-47    Safety Code, are amended to read as follows:

15-48          (h)  A pharmacist may dispense a controlled substance listed

15-49    in Schedule III, IV, or V under an original written prescription

15-50    issued by a practitioner  defined by Section 481.002(39)(C)

15-51    [481.002(38)(C)] and only if the pharmacist determines that the

15-52    prescription was issued for a valid  medical purpose and in the

15-53    course of professional practice.  A prescription issued under this

15-54    subsection may not be filled or refilled later than six  months

15-55    after the date the prescription is issued, and a prescription

15-56    authorized to be refilled on the original prescription may not be

15-57    refilled more  than five times.

15-58          (i)  A person may not dispense a controlled substance listed

15-59    in Schedule V and containing 200 milligrams or less of codeine, or

15-60    any of its salts, per 100 milliliters or per 100 grams, or

15-61    containing 100 milligrams or less of dihydrocodeine, or any of its

15-62    salts, per 100 milliliters or per 100 grams, [Section 481.036(1) or

15-63    (2)] without the prescription of a  practitioner defined by Section

15-64    481.002(39)(A), except that a practitioner may dispense the

15-65    substance directly to an ultimate user. A prescription  issued

15-66    under this subsection may not be filled or refilled later than six

15-67    months after the date the prescription is issued and may not be

15-68    refilled  more than five times, unless the prescription is renewed

15-69    by the practitioner.

 16-1          (k)  A prescription for a controlled substance must show:

 16-2                (1)  the quantity of the substance prescribed:

 16-3                      (A)  numerically, followed by the number written

 16-4    as a word, if the prescription is written; or

 16-5                      (B)  if the prescription is communicated orally

 16-6    or telephonically, as transcribed by the receiving pharmacist;

 16-7                (2)  the date of issue;

 16-8                (3)  the name and address of the patient or, if the

 16-9    controlled substance is prescribed for an animal, the species of

16-10    the animal and the name and address of its owner;

16-11                (4)  the name and strength of the controlled substance

16-12    prescribed;

16-13                (5)  the directions for use of the controlled

16-14    substance;

16-15                [(6)  the legibly stamped or printed name, address,

16-16    Federal Drug Enforcement Administration registration number, and

16-17    telephone number of the practitioner at the practitioner's usual

16-18    place of business.]

16-19                (6)  the intended use of the substance prescribed

16-20    [drug] unless the practitioner determines the furnishing of this

16-21    information is not in the best interest of the patient; and

16-22                (7)  the legibly printed or stamped name, address,

16-23    Federal Drug Enforcement Administration registration number, and

16-24    telephone number of the practitioner at the practitioner's usual

16-25    place of business[, legibly printed or stamped].

16-26          SECTION 10.  Sections 481.077(a), (b), (c), (k), and (l),

16-27    Health and Safety Code, are amended to read as follows:

16-28          (a)  Except as provided by Subsection (l), a person who

16-29    sells, transfers, or otherwise furnishes any of the following

16-30    precursor substances to a person  shall make an accurate and

16-31    legible record of the transaction and maintain the record for at

16-32    least two years after the date of the transaction:

16-33                (1)  Methylamine;

16-34                (2)  Ethylamine;

16-35                (3)  D-lysergic acid;

16-36                (4)  Ergotamine tartrate;

16-37                (5)  Diethyl malonate;

16-38                (6)  Malonic acid;

16-39                (7)  Ethyl malonate;

16-40                (8)  Barbituric acid;

16-41                (9)  Piperidine;

16-42                (10)  N-acetylanthranilic acid;

16-43                (11)  Pyrrolidine;

16-44                (12)  Phenylacetic acid;

16-45                (13)  Anthranilic acid;

16-46                (14)  [Morpholine;]

16-47                [(15)]  Ephedrine;

16-48                (15) [(16)]  Pseudoephedrine;

16-49                (16)  Norpseudoephedrine [or norpseudoephedrine]; or

16-50                (17)  Phenylpropanolamine.

16-51          (b)  The director by rule may:

16-52                (1)  name an additional chemical substance as a

16-53    precursor  [substances as precursors] for purposes of Subsection

16-54    (a) if  the director determines that public health and welfare are

16-55    jeopardized by evidenced proliferation or use of the [a chemical]

16-56    substance [used] in the illicit manufacture of a controlled

16-57    substance or controlled substance analogue; or

16-58                (2)  [. The director by rule may] delete a substance

16-59    listed in [named as a precursor for purposes of] Subsection (a)  if

16-60    the director determines that the substance does not jeopardize

16-61    public health and welfare or is not used in the illicit manufacture

16-62    of a controlled  substance or a controlled substance analogue.

16-63          (c)  This section and Section 481.078 do not apply to a

16-64    person to whom a registration has been issued under Section 481.063

16-65    [The Department of Public Safety shall file with the secretary of

16-66    state a certified copy of a rule adopted under this section].

16-67          (k)  Unless the person is the holder of only a permit issued

16-68    under Section 481.078(b)(1), a [A] manufacturer, wholesaler,

16-69    retailer, or other person who sells, transfers, or otherwise

 17-1    furnishes any substance subject to Subsection (a) or a permit

 17-2    holder, commercial  purchaser, or other person who receives a

 17-3    substance governed by Subsection (a):

 17-4                (1)  shall maintain records and inventories in

 17-5    accordance with rules established by the director;

 17-6                (2)  [and] shall allow a member of the Department of

 17-7    Public Safety or a peace officer to conduct audits and inspect

 17-8    records of purchases and sales and all other records made in

 17-9    accordance with this section at any reasonable time; and

17-10                (3)  may not interfere with the audit or with the full

17-11    and complete inspection or copying of those records [.  This

17-12    subsection does not apply to a recipient who has obtained a

17-13    precursor substance subject to Subsection (a) and who is a permit

17-14    holder under Section 481.078].

17-15          (l)  This section does not apply to the sale or transfer of a

17-16    nonnarcotic product that includes a precursor substance subject to

17-17    Subsection (a) if the  sale or transfer complies with federal law

17-18    and involves a product that may be sold lawfully with a

17-19    prescription or over the counter without a prescription under the

17-20    Federal Food, Drug, and Cosmetic Act (21 U.S.C. Section 301 et

17-21    seq.) or a rule adopted under that Act.

17-22          SECTION 11.  Section 481.078, Health and Safety Code, is

17-23    amended by amending Subsections (b) and (e) and adding Subsection

17-24    (f) to read as  follows:

17-25          (b)  The director [Department of Public Safety] by rule shall

17-26    adopt [develop] procedures and standards for the issuance and

17-27    renewal or the voluntary surrender, cancellation, suspension,

17-28    probation, or revocation of:

17-29                (1)  a permit for one sale, transfer, receipt, or

17-30    otherwise furnishing of a controlled substance precursor; or

17-31                (2)  a permit for more than one sale, transfer,

17-32    receipt, or otherwise furnishing of a controlled substance

17-33    precursor.

17-34          (e)  The director may not issue a permit under this section

17-35    unless the person applying for the permit delivers to the director

17-36    a written consent to inspect signed by the person that grants to

17-37    the  director the right to inspect any controlled premises, record,

17-38    chemical precursor, or other item governed by this chapter in the

17-39    care, custody, or control of the person.  After the director

17-40    receives the consent, the director may inspect any controlled

17-41    premises, record, chemical precursor, or other item to which the

17-42    consent applies.

17-43          (f)  The director may adopt rules to establish security

17-44    controls and provide for the inspection of a place, entity, or item

17-45    to which a chemical  precursor transfer permit applies.

17-46    [Department of Public Safety shall file with the secretary of state

17-47    a certified copy of a rule adopted under this section.]

17-48          SECTION 12.  Sections 481.080(a), (d), (e), and (m), Health

17-49    and Safety Code, are amended  to read as follows:

17-50          (a)  In this section, "chemical laboratory apparatus" means

17-51    any item of equipment designed, made, or adapted to manufacture a

17-52    controlled substance or a controlled substance analogue, including:

17-53                (1)  a condenser [condensers];

17-54                (2)  a distilling apparatus;

17-55                (3)  a vacuum drier [dryers];

17-56                (4)  a three-neck or [flasks;]

17-57                [(5)]  distilling flask;

17-58                (5)  a [flasks;]

17-59                [(6)]  tableting machine;

17-60                (6)  an [machines; or]

17-61                [(7)]  encapsulating machine;

17-62                (7)  a filter, Buchner, or separatory funnel;

17-63                (8)  an Erlenmeyer, two-neck, or single-neck flask;

17-64                (9)  a round-bottom, Florence, thermometer, or

17-65    filtering flask;

17-66                (10)  a Soxhlet extractor;

17-67                (11)  a transformer;

17-68                (12)  a flask heater;

17-69                (13)  a heating mantel; or

 18-1                (14)  an adaptor tube [machines].

 18-2          (d)  The director by rule may:

 18-3                (1)  name additional chemical laboratory apparatus for

 18-4    purposes of Subsection (a) if the director determines that public

 18-5    health and  welfare are jeopardized by evidenced proliferation or

 18-6    use of a chemical laboratory apparatus in the illicit manufacture

 18-7    of a controlled  substance or controlled substance analogue; or

 18-8                (2)  [.  The director by rule may] delete an apparatus

 18-9    listed in Subsection (a) if the director determines that the

18-10    apparatus does  not jeopardize public health and welfare or is not

18-11    used in the illicit manufacture of a controlled substance or a

18-12    controlled substance analogue.

18-13          (e)  This section and Section 481.081 do not apply to a

18-14    person to whom a registration has been issued under Section 481.063

18-15    [The Department of Public Safety shall file with the secretary of

18-16    state a  certified copy of a rule adopted under this section].

18-17          (m)  This subsection applies to a [A] manufacturer,

18-18    wholesaler, retailer, or other person who sells, transfers, or

18-19    otherwise furnishes  any apparatus subject to Subsection (a) and to

18-20    a permit holder, commercial purchaser, or other person who receives

18-21    an apparatus governed by  Subsection (a) unless the person is the

18-22    holder of only a permit issued under Section 481.081(b)(1).  A

18-23    person covered by this subsection:

18-24                (1)  shall maintain records and inventories in

18-25    accordance with rules established by the director;

18-26                (2)  [and] shall allow a member of the Department of

18-27    Public Safety or a peace officer to conduct audits and inspect

18-28    records of purchases and sales and all other records made in

18-29    accordance with this section at any reasonable time; and

18-30                (3)  may not interfere with the audit or with the full

18-31    and complete inspection or copying of those records [. This

18-32    subsection does not  apply to a recipient who has obtained a

18-33    chemical laboratory apparatus subject to Subsection (a) and who is

18-34    a permit holder under Section 481.081].

18-35          SECTION 13.  Section 481.081, Health and Safety Code, is

18-36    amended by amending Subsections (b) and (e) and adding Subsection

18-37    (f) to read as  follows:

18-38          (b)  The director [Department of Public Safety] by rule shall

18-39    adopt [develop] procedures and standards for the issuance and

18-40    renewal or the voluntary surrender, cancellation, suspension,

18-41    probation, or revocation of:

18-42                (1)  a permit for one sale, transfer, receipt, or

18-43    otherwise furnishing of a chemical laboratory apparatus; or

18-44                (2)  a permit for more than one sale, transfer,

18-45    receipt, or otherwise furnishing of a chemical laboratory

18-46    apparatus.

18-47          (e)  The director may not issue a permit under this section

18-48    unless the person applying for the permit delivers to the director

18-49    a written consent to inspect signed by the person that grants to

18-50    the  director the right to inspect any controlled premises, record,

18-51    chemical laboratory apparatus, or other item governed by this

18-52    chapter in the care, custody, or control of the person.  After the

18-53    director receives the consent, the director may inspect any

18-54    controlled premises, record, chemical laboratory apparatus, or

18-55    other item to which the consent applies.

18-56          (f)  The director may by rule establish security controls and

18-57    provide for the inspection of a place, entity, or item to which a

18-58    chemical laboratory apparatus transfer permit applies.  [Department

18-59    of Public Safety shall file with the secretary of state a certified

18-60    copy of a rule adopted under this section.]

18-61          SECTION 14.  Section 481.102, Health and Safety Code, is

18-62    amended to read as follows:

18-63          Sec. 481.102.  PENALTY GROUP 1.  Penalty Group 1 consists of:

18-64                (1)  the following opiates, including their isomers,

18-65    esters, ethers, salts, and salts of isomers, esters, and ethers,

18-66    unless specifically excepted,  if the existence of these isomers,

18-67    esters, ethers, and salts is possible within the specific chemical

18-68    designation:

18-69                      Alfentanil;

 19-1                      Allylprodine;

 19-2                      Alphacetylmethadol;

 19-3                      Benzethidine;

 19-4                      Betaprodine;

 19-5                      Clonitazene;

 19-6                      Diampromide;

 19-7                      Diethylthiambutene;

 19-8                      Difenoxin not listed in Penalty Group 3 or 4;

 19-9                      Dimenoxadol;

19-10                      Dimethylthiambutene;

19-11                      Dioxaphetyl butyrate;

19-12                      Dipipanone;

19-13                      Ethylmethylthiambutene;

19-14                      Etonitazene;

19-15                      Etoxeridine;

19-16                      Furethidine;

19-17                      Hydroxypethidine;

19-18                      Ketobemidone;

19-19                      Levophenacylmorphan;

19-20                      Meprodine;

19-21                      Methadol;

19-22                      Moramide;

19-23                      Morpheridine;

19-24                      Noracymethadol;

19-25                      Norlevorphanol;

19-26                      Normethadone;

19-27                      Norpipanone;

19-28                      Phenadoxone;

19-29                      Phenampromide;

19-30                      Phenomorphan;

19-31                      Phenoperidine;

19-32                      Piritramide;

19-33                      Proheptazine;

19-34                      Properidine;

19-35                      Propiram;

19-36                      Sufentanil;

19-37                      Tilidine; and

19-38                      Trimeperidine;

19-39                (2)  the following opium derivatives, their salts,

19-40    isomers, and salts of isomers, unless specifically excepted, if the

19-41    existence of these salts,  isomers, and salts of isomers is

19-42    possible within the specific chemical designation:

19-43                      Acetorphine;

19-44                      Acetyldihydrocodeine;

19-45                      Benzylmorphine;

19-46                      Codeine methylbromide;

19-47                      Codeine-N-Oxide;

19-48                      Cyprenorphine;

19-49                      Desomorphine;

19-50                      Dihydromorphine;

19-51                      Drotebanol;

19-52                      Etorphine, except hydrochloride salt;

19-53                      Heroin;

19-54                      Hydromorphinol;

19-55                      Methyldesorphine;

19-56                      Methyldihydromorphine;

19-57                      Monoacetylmorphine;

19-58                      Morphine methylbromide;

19-59                      Morphine methylsulfonate;

19-60                      Morphine-N-Oxide;

19-61                      Myrophine;

19-62                      Nicocodeine;

19-63                      Nicomorphine;

19-64                      Normorphine;

19-65                      Pholcodine; and

19-66                      Thebacon;

19-67                (3)  the following substances, however produced, except

19-68    those narcotic drugs listed in another group:

19-69                      (A)  Opium and opiate not listed in Penalty Group

 20-1    3 or 4, and a salt, compound, derivative, or preparation of opium

 20-2    or opiate, other than  thebaine derived butorphanol, nalmefene and

 20-3    its salts, naloxone and its salts, and naltrexone and its salts,

 20-4    but including:

 20-5                            Codeine not listed in Penalty Group 3 or 4;

 20-6                            Ethylmorphine not listed in Penalty Group 3

 20-7    or 4;

 20-8                            Granulated opium;

 20-9                            Hydrocodone not listed in Penalty Group 3;

20-10                            Hydromorphone;

20-11                            Metopon;

20-12                            Morphine not listed in Penalty Group 3;

20-13                            Opium extracts;

20-14                            Opium fluid extracts;

20-15                            Oxycodone;

20-16                            Oxymorphone;

20-17                            Powdered opium;

20-18                            Raw opium;

20-19                            Thebaine; and

20-20                            Tincture of opium;

20-21                      (B)  a salt, compound, isomer, derivative, or

20-22    preparation of a substance that is chemically equivalent or

20-23    identical to a substance described by  Paragraph (A), other than

20-24    the isoquinoline alkaloids of opium;

20-25                      (C)  Opium poppy and poppy straw;

20-26                      (D)  Cocaine, including:

20-27                            (i)  its salts, its optical, position, and

20-28    geometric isomers, and the salts of those isomers;

20-29                            (ii)  coca leaves and a salt, compound,

20-30    derivative, or preparation of coca leaves;

20-31                            (iii)  a salt, compound, derivative, or

20-32    preparation of a salt, compound, or derivative that is chemically

20-33    equivalent or identical to a  substance described by Subparagraph

20-34    (i) or (ii), other than decocainized coca leaves or extractions of

20-35    coca leaves that do not contain cocaine or  ecgonine; and

20-36                      (E)  concentrate of poppy straw, meaning the

20-37    crude extract of poppy straw in liquid, solid, or powder form that

20-38    contains the phenanthrine  alkaloids of the opium poppy[; and]

20-39                      [(F)  temporary listing of substances subject to

20-40    emergency scheduling by the Federal Drug Enforcement

20-41    Administration];

20-42                (4)  the following opiates, including their isomers,

20-43    esters, ethers, salts, and salts of isomers, if the existence of

20-44    these isomers, esters, ethers, and salts is possible within the

20-45    specific chemical designation:

20-46                      Acetyl-alpha-methylfentanyl

20-47    (N-(1-(1-methyl-2-phenethyl)-4-piperidinyl)-N-phenylacetamide);

20-48                      Alpha-methylthiofentanyl

20-49    (N-(1-methyl-2-(2-thienyl)ethyl-4-piperidinyl)-N-phenylpropanamide);

20-50                      Alphaprodine;

20-51                      Anileridine;

20-52                      Beta-hydroxyfentanyl

20-53    (N-(1-(2-hydroxy-2-phenethyl)-4-piperidinyl)-N-phenylpropanamide);

20-54                      Beta-hydroxy-3-methylfentanyl;

20-55                      Bezitramide;

20-56                      Carfentanil;

20-57                      Dihydrocodeine not listed in Penalty Group 3 or

20-58    4;

20-59                      Diphenoxylate not listed in Penalty Group 3 or 4;

20-60                      Fentanyl or alpha-methylfentanyl, or any other

20-61    derivative of Fentanyl;

20-62                      Isomethadone;

20-63                      Levomethorphan;

20-64                      Levorphanol;

20-65                      Metazocine;

20-66                      Methadone;

20-67                      Methadone-Intermediate,

20-68    4-cyano-2-dimethylamino-4, 4-diphenyl butane;

20-69                      3-methylfentanyl(N-(3-methyl-1-(2-phenylethyl)-

 21-1    4-piperidyl)-N-phenylpropanamide);

 21-2                      3-methylthiofentanyl(N-(3-methyl-1-(2-thienyl)

 21-3    ethyl-4-piperidinyl[piperidyl])-N-phenylpropanamide);

 21-4                      Moramide-Intermediate, 2-methyl-3-morpholino-1,

 21-5    1-diphenyl-propane-carboxylic acid;

 21-6                      Para-fluorofentanyl(N-(4-fluorophenyl)-N-(1-

 21-7    (2-phenylethyl)-4-piperidinyl)propanamide);

 21-8                      PEPAP

 21-9    (1-(2-phenethyl)-4-phenyl-4-acetoxypiperidine);

21-10                      Pethidine (Meperidine);

21-11                      Pethidine-Intermediate-A,

21-12    4-cyano-1-methyl-4-phenylpiperidine;

21-13                      Pethidine-Intermediate-B,

21-14    ethyl-4-phenylpiperidine-4 carboxylate;

21-15                      Pethidine-Intermediate-C,

21-16    1-methyl-4-phenylpiperidine-4-carboxylic acid;

21-17                      Phenazocine;

21-18                      Piminodine;

21-19                      Racemethorphan;

21-20                      Racemorphan; and

21-21                      Thiofentanyl(N-phenyl-N-(1-(2-thienyl)ethyl-4-

21-22    piperidinyl)-propanamide);

21-23                (5)  Flunitrazepam (some trade or other names:

21-24    Rohypnol) [Lysergic acid diethylamide, including its salts,

21-25    isomers, and salts of isomers];

21-26                (6)  Methamphetamine, including its salts, optical

21-27    isomers, and salts of optical isomers;

21-28                (7)  Phenylacetone and methylamine, if possessed

21-29    together with intent to manufacture methamphetamine; [and]

21-30                (8)  Phencyclidine, including its salts; and

21-31                (9)  Gamma hydroxybutyrate, including its salts.

21-32          SECTION 15.  Subchapter D, Chapter 481, Health and Safety

21-33    Code, is amended by adding Section 481.1021 to read as follows:

21-34          Sec. 481.1021.  PENALTY GROUP 1-A.   Penalty Group 1-A

21-35    consists of lysergic acid diethylamide (LSD), including its salts,

21-36    isomers, and salts of  isomers.

21-37          SECTION 16.  Section 481.103, Health and Safety Code, is

21-38    amended to read as follows:

21-39          Sec. 481.103.  PENALTY GROUP 2.  (a)  Penalty Group 2

21-40    consists of:

21-41                (1)  any quantity of the following hallucinogenic

21-42    substances, their salts, isomers, and salts of isomers, unless

21-43    specifically excepted, if the  existence of these salts, isomers,

21-44    and salts of isomers is possible within the specific chemical

21-45    designation:

21-46                      alpha-ethyltryptamine;

21-47                      4-bromo-2, 5-dimethoxyamphetamine (some trade or

21-48    other names:  4-bromo-2, 5-dimethoxy-alpha-methylphenethylamine;

21-49    4-bromo-2, 5-DMA);

21-50                      4-bromo-2, 5-dimethoxyphenethylamine;

21-51                      Bufotenine (some trade and other names:

21-52    3-(beta-Dimethylaminoethyl)-5-hydroxyindole;

21-53    3-(2-dimethylaminoethyl)-5- indolol; N, N-dimethylserotonin;

21-54    5-hydroxy-N, N-dimethyltryptamine; mappine);

21-55                      Diethyltryptamine (some trade and other names:

21-56    N, N-Diethyltryptamine, DET);

21-57                      2, 5-dimethoxyamphetamine (some trade or other

21-58    names:  2, 5-dimethoxy-alpha-methylphenethylamine; 2, 5-DMA);

21-59                      2, 5-dimethoxy-4-ethylamphetamine (some trade or

21-60    other names: DOET);

21-61                      Dimethyltryptamine (some trade and other names:

21-62    DMT);

21-63                      Dronabinol (synthetic) in sesame oil and

21-64    encapsulated in a soft gelatin capsule in a U.S. Food and Drug

21-65    Administration approved drug product (some  trade or other names

21-66    for Dronabinol:  (a6aR-trans)-6a,7,8,10a-tetrahydro-

21-67    6,6,9-trimethyl-3-pentyl-6H- dibenzo (b,d)pyran-1-ol or

21-68    (-)-delta-9-(trans)-tetrahydrocannabinol);

21-69                      Ethylamine Analog of Phencyclidine (some trade or

 22-1    other names:  N-ethyl-1-phenylcyclohexylamine, (1-phenylcyclohexyl)

 22-2    ethylamine,  N-(1-phenylcyclohexyl) ethylamine, cyclohexamine,

 22-3    PCE);

 22-4                      Ibogaine (some trade or other names:  7-Ethyl-6,

 22-5    6, beta 7, 8, 9, 10, 12, 13-octahydro-2-methoxy-6,

 22-6    9-methano-5H-pyrido (1', 2':1, 2) azepino (5,  4-b) indole;

 22-7    tabernanthe iboga.);

 22-8                      Mescaline;

 22-9                      5-methoxy-3, 4-methylenedioxy amphetamine;

22-10                      4-methoxyamphetamine (some trade or other names:

22-11    4-methoxy-alpha-methylphenethylamine; paramethoxyamphetamine; PMA);

22-12                      1-methyl- 4-phenyl-4-propionoxypiperidine (MPPP,

22-13    PPMP);

22-14                      4-methyl-2, 5-dimethoxyamphetamine (some trade

22-15    and other names:  4-methyl-2,

22-16    5-dimethoxy-alpha-methylphenethylamine; "DOM"; "STP");

22-17                      3,4-methylenedioxy methamphetamine (MDMA, MDM);

22-18                      3,4-methylenedioxy amphetamine;

22-19                      3,4-methylenedioxy N-ethylamphetamine (Also known

22-20    as N-ethyl MDA);

22-21                      Nabilone (Another name for nabilone:

22-22    (+)-trans-3-(1,1-dimethylheptyl)- 6,6a,7,8,10,10a-hexahydro-1-

22-23    hydroxy-6,6-dimethyl-9H-dibenzo(b,d)pyran-9-one;

22-24                      N-ethyl-3-piperidyl benzilate;

22-25                      N-hydroxy-3,4-methylenedioxyamphetamine (Also

22-26    known as N-hydroxy MDA);

22-27                      4-methylaminorex;

22-28                      N-methyl-3-piperidyl benzilate;

22-29                      Parahexyl (some trade or other names:

22-30    3-Hexyl-1-hydroxy-7, 8, 9, 10-tetrahydro-6, 6,

22-31    9-trimethyl-6H-dibenzo (b, d) pyran;  Synhexyl);

22-32                      1-Phenylcyclohexylamine;

22-33                      1-Piperidinocyclohexanecarbonitrile (PCC);

22-34                      Psilocin;

22-35                      Psilocybin;

22-36                      Pyrrolidine Analog of Phencyclidine (some trade

22-37    or other names: 1-(1-phenylcyclohexyl)-pyrrolidine, PCPy, PHP);

22-38                      Tetrahydrocannabinols, other than marihuana, and

22-39    synthetic equivalents of the substances contained in the plant, or

22-40    in the resinous extractives of  Cannabis, or synthetic substances,

22-41    derivatives, and their isomers with similar chemical structure and

22-42    pharmacological activity such as:

22-43                            delta-1 cis or trans tetrahydrocannabinol,

22-44    and their optical isomers;

22-45                            delta-6 cis or trans tetrahydrocannabinol,

22-46    and their optical isomers;

22-47                            delta-3, 4 cis or trans

22-48    tetrahydrocannabinol, and its optical isomers;

22-49                            compounds of these structures, regardless

22-50    of numerical designation of atomic positions, since nomenclature of

22-51    these substances is not  internationally standardized;

22-52                      Thiophene Analog of Phencyclidine (some trade or

22-53    other names:  1-(1-(2-thienyl) cyclohexyl) piperidine; 2-Thienyl

22-54    Analog of Phencyclidine;  TPCP,  TCP);

22-55                      1-(1-(2-thienyl)cyclohexyl)pyrrolidine (some

22-56    trade or other names:  TCPy); and

22-57                      3,4,5-trimethoxy amphetamine;

22-58                (2)  Phenylacetone (some trade or other names:

22-59    Phenyl-2-propanone; P2P [P-2-P], Benzymethyl ketone, methyl benzyl

22-60    ketone); and

22-61                (3)  unless specifically excepted or unless listed in

22-62    another Penalty Group, a material, compound, mixture, or

22-63    preparation that contains any  quantity of the following substances

22-64    having a potential for abuse associated with a depressant or

22-65    stimulant effect on the central nervous system:

22-66                      Aminorex (some trade or other names:

22-67    aminoxaphen; 2-amino-5-phenyl-2-oxazoline;

22-68    4,5-dihydro-5-phenyl-2-oxazolamine);

22-69                      Amphetamine, its salts, optical isomers, and

 23-1    salts of optical isomers;

 23-2                      Cathinone (some trade or other names:

 23-3    2-amino-1-phenyl-1-propanone, alpha-aminopropiophenone,

 23-4    2-aminopropiophenone);

 23-5                      Etorphine Hydrochloride;

 23-6                      Fenethylline and its salts;

 23-7                      Mecloqualone and its salts;

 23-8                      Methaqualone and its salts;

 23-9                      Methcathinone (some trade or other names:

23-10    2-methylamino-propiophenone; alpha-(methylamino)propriophenone;

23-11    2-(methylamino)-1-phenylpropan-1-one;

23-12    alpha-N-methylaminopropriophenone; monomethylpropion; ephedrone,

23-13    N-methylcathinone; methylcathinone; AL-464; AL-422; AL-463; and UR

23-14    1431);

23-15                      N-Ethylamphetamine, its salts, optical isomers,

23-16    and salts of optical isomers; and

23-17                      N,N-dimethylamphetamine (some trade or other

23-18    names:  N,N,alpha-trimethylbenzeneethaneamine;

23-19    N,N,alpha-trimethylphenethylamine), its salts, optical isomers, and

23-20    salts of optical isomers.

23-21          (b)  For the purposes of Subsection (a)(1) only, the term

23-22    "isomer" includes an optical, position, or geometric isomer.

23-23          SECTION 17.  Section 481.104,  Health and Safety Code, is

23-24    amended to read as follows:

23-25          Sec. 481.104.  PENALTY GROUP 3.  (a)  Penalty Group 3

23-26    consists of:

23-27                (1)  a material, compound, mixture, or preparation that

23-28    contains any quantity of the following substances having a

23-29    potential for abuse associated  with a stimulant effect on the

23-30    central nervous system:

23-31                      Methylphenidate and its salts; and

23-32                      Phenmetrazine and its salts;

23-33                (2)  a material, compound, mixture, or preparation that

23-34    contains any quantity of the following substances having a

23-35    potential for abuse associated  with a depressant effect on the

23-36    central nervous system:

23-37                      a substance that contains any quantity of a

23-38    derivative of barbituric acid, or any salt of a derivative of

23-39    barbituric acid not otherwise covered by  this subsection;

23-40                      a compound, mixture, or preparation containing

23-41    amobarbital, secobarbital, pentobarbital, or any salt of any of

23-42    these, and one or more active  medicinal ingredients that are not

23-43    listed in any penalty group;

23-44                      a suppository dosage form containing amobarbital,

23-45    secobarbital, pentobarbital, or any salt of any of these drugs, and

23-46    approved by the United States Food and Drug Administration for

23-47    marketing only as a suppository;

23-48                      Alprazolam;

23-49                      Amobarbital;

23-50                      Bromazepam;

23-51                      Camazepam;

23-52                      Chlordiazepoxide;

23-53                      Chlorhexadol;

23-54                      Clobazam;

23-55                      Clonazepam;

23-56                      Clorazepate;

23-57                      Clotiazepam;

23-58                      Cloxazolam;

23-59                      Delorazepam;

23-60                      Diazepam;

23-61                      Estazolam;

23-62                      Ethyl loflazepate;

23-63                      Fludiazepam;

23-64                      [Flunitrazepam;]

23-65                      Flurazepam;

23-66                      Glutethimide;

23-67                      Halazepam;

23-68                      Haloxzolam;

23-69                      Ketazolam;

 24-1                      Loprazolam;

 24-2                      Lorazepam;

 24-3                      Lormetazepam;

 24-4                      Lysergic acid, including its salts, isomers, and

 24-5    salts of isomers;

 24-6                      Lysergic acid amide, including its salts,

 24-7    isomers, and salts of isomers;

 24-8                      Mebutamate;

 24-9                      Medazepam;

24-10                      Methyprylon;

24-11                      Midazolam;

24-12                      Nimetazepam;

24-13                      Nitrazepam;

24-14                      Nordiazepam;

24-15                      Oxazepam;

24-16                      Oxazolam;

24-17                      Pentazocine, its salts, derivatives, or compounds

24-18    or mixtures thereof;

24-19                      Pentobarbital;

24-20                      Pinazepam;

24-21                      Prazepam;

24-22                      Quazepam;

24-23                      Secobarbital;

24-24                      Sulfondiethylmethane;

24-25                      Sulfonethylmethane;

24-26                      Sulfonmethane;

24-27                      Temazepam;

24-28                      Tetrazepam;

24-29                      Tiletamine and zolazepam in combination, and its

24-30    salts. (some trade or other names for a tiletamine-zolazepam

24-31    combination product:  Telazol, for  tiletamine:

24-32    2-(ethylamino)-2-(2-thienyl)-cyclohexanone, and for zolazepam:

24-33    4-(2-fluorophenyl)-6,

24-34    8-dihydro-1,3,8,-trimethylpyrazolo-(3,4-e)(1,4)-d

24-35    diazepin-7(1H)-one, flupyrazapon); [and]

24-36                      Triazolam; and

24-37                      Zolpidem;

24-38                (3)  Nalorphine;

24-39                (4)  a material, compound, mixture, or preparation

24-40    containing limited quantities of the following narcotic drugs, or

24-41    any of their salts:

24-42                      not more than 1.8 grams of codeine, or any of its

24-43    salts, per 100 milliliters or not more than 90 milligrams per

24-44    dosage unit, with an equal or  greater quantity of an isoquinoline

24-45    alkaloid of opium;

24-46                      not more than 1.8 grams of codeine, or any of its

24-47    salts, per 100 milliliters or not more than 90 milligrams per

24-48    dosage unit, with one or more  active, nonnarcotic ingredients in

24-49    recognized therapeutic amounts;

24-50                      not more than 300 milligrams of dihydrocodeinone

24-51    (hydrocodone), or any of its salts, per 100 milliliters or not more

24-52    than 15 milligrams per  dosage unit, with a fourfold or greater

24-53    quantity of an isoquinoline alkaloid of opium;

24-54                      not more than 300 milligrams of dihydrocodeinone

24-55    (hydrocodone), or any of its salts, per 100 milliliters or not more

24-56    than 15 milligrams per  dosage unit, with one or more active,

24-57    nonnarcotic ingredients in recognized therapeutic amounts;

24-58                      not more than 1.8 grams of dihydrocodeine, or any

24-59    of its salts, per 100 milliliters or not more than 90 milligrams

24-60    per dosage unit, with one or  more active, nonnarcotic ingredients

24-61    in recognized therapeutic amounts;

24-62                      not more than 300 milligrams of ethylmorphine, or

24-63    any of its salts, per 100 milliliters or not more than 15

24-64    milligrams per dosage unit, with one or more active, nonnarcotic

24-65    ingredients in recognized therapeutic amounts;

24-66                      not more than 500 milligrams of opium per 100

24-67    milliliters or per 100 grams, or not more than 25 milligrams per

24-68    dosage unit, with one or more  active, nonnarcotic ingredients in

24-69    recognized therapeutic amounts;

 25-1                      not more than 50 milligrams of morphine, or any

 25-2    of its salts, per 100 milliliters or per 100 grams with one or more

 25-3    active, nonnarcotic ingredients in recognized therapeutic amounts;

 25-4    and

 25-5                      not more than 1 milligram of difenoxin and not

 25-6    less than 25 micrograms of atropine sulfate per dosage unit;

 25-7                (5)  a material, compound, mixture, or preparation that

 25-8    contains any quantity of the following substances:

 25-9                      Barbital;

25-10                      Chloral betaine;

25-11                      Chloral hydrate;

25-12                      Ethchlorvynol;

25-13                      Ethinamate;

25-14                      Meprobamate;

25-15                      Methohexital;

25-16                      Methylphenobarbital (Mephobarbital);

25-17                      Paraldehyde;

25-18                      Petrichloral; and

25-19                      Phenobarbital;

25-20                (6)  Peyote, unless unharvested and growing in its

25-21    natural state, meaning all parts of the plant classified

25-22    botanically as Lophophora, whether growing or not, the seeds of the

25-23    plant, an extract from a part of the plant, and every compound,

25-24    manufacture, salt, derivative, mixture, or preparation of the

25-25    plant, its seeds, or extracts;

25-26                (7)  unless listed in another penalty group, a

25-27    material, compound, mixture, or preparation that contains any

25-28    quantity of the following substances having a stimulant effect on

25-29    the central nervous system, including the substance's salts,

25-30    optical, position, or geometric isomers, and salts of the

25-31    substance's isomers, if the existence of the salts, isomers, and

25-32    salts of isomers is possible within the specific chemical

25-33    designation:

25-34                      Benzphetamine;

25-35                      Cathine ((+)-norpseudoephedrine);

25-36                      Chlorphentermine;

25-37                      Clortermine;

25-38                      Diethylpropion;

25-39                      Fencamfamin;

25-40                      Fenfluramine;

25-41                      Fenproporex;

25-42                      Mazindol;

25-43                      Mefenorex;

25-44                      Pemoline (including organometallic complexes and

25-45    their chelates);

25-46                      Phendimetrazine;

25-47                      Phentermine;

25-48                      Pipradrol; and

25-49                      SPA ((-)-1-dimethylamino-1,2-diphenylethane);

25-50                (8)  unless specifically excepted or unless listed in

25-51    another penalty group, a material, compound, mixture, or

25-52    preparation that contains any quantity of the following substance,

25-53    including its salts:

25-54                      Dextropropoxyphene

25-55    (Alpha-(+)-4-dimethylamino-1,2-diphenyl-3-methyl-2-propionoxybutane);

25-56    and

25-57                (9)  an anabolic steroid or any substance that is

25-58    chemically or pharmacologically related to testosterone, other than

25-59    an estrogen, progestin, or corticosteroid, and promotes muscle

25-60    growth, including [any human growth hormone or any of the following

25-61    anabolic steroids, or any isomer, ester, salt, or derivative of the

25-62    following that acts in the same manner on the human body]:

25-63                      Boldenone;

25-64                      Chlorotestosterone (4-chlortestosterone);

25-65                      Clostebol;

25-66                      Dehydrochlormethyltestosterone;

25-67                      Dihydrotestosterone (4-dihydrotestosterone);

25-68                      Drostanolone;

25-69                      Ethylestrenol;

 26-1                      Fluoxymesterone;

 26-2                      Formebulone;

 26-3                      Mesterolone;

 26-4                      Methandienone;

 26-5                      Methandranone;

 26-6                      Methandriol;

 26-7                      Methandrostenolone;

 26-8                      Methenolone;

 26-9                      Methyltestosterone;

26-10                      Mibolerone;

26-11                      Nandrolone;

26-12                      Norethandrolone;

26-13                      Oxandrolone;

26-14                      Oxymesterone;

26-15                      Oxymetholone;

26-16                      Stanolone;

26-17                      Stanozolol;

26-18                      Testolactone;

26-19                      Testosterone; and

26-20                      Trenbolone.

26-21          (b)  Penalty Group 3 does not include a compound, mixture, or

26-22    preparation containing a stimulant substance listed in Subsection

26-23    (a)(1) if the compound, mixture, or preparation contains one or

26-24    more active medicinal ingredients not having a stimulant effect on

26-25    the central nervous system and if the admixtures are included in

26-26    combinations, quantity, proportion, or concentration that vitiate

26-27    the potential for abuse of the substances that have a stimulant

26-28    effect on the central nervous system.

26-29          (c)  Penalty Group 3 does not include a compound, mixture, or

26-30    preparation containing a depressant substance listed in Subsection

26-31    (a)(2) or (a)(5) if the compound, mixture, or preparation contains

26-32    one or more active medicinal ingredients not having a depressant

26-33    effect on the central nervous system and if the admixtures are

26-34    included in combinations, quantity, proportion, or concentration

26-35    that vitiate the potential for abuse of the substances that have a

26-36    depressant effect on the central nervous system.

26-37          SECTION 18.  Section 481.105, Health and Safety Code, is

26-38    amended to read as follows:

26-39          Sec. 481.105.  PENALTY GROUP 4.  Penalty Group 4 consists of:

26-40                (1)  a compound, mixture, or preparation containing

26-41    limited quantities of any of the following narcotic drugs that

26-42    includes one or more nonnarcotic active medicinal ingredients in

26-43    sufficient proportion to confer on the compound, mixture, or

26-44    preparation valuable medicinal qualities other than those possessed

26-45    by the narcotic drug alone:

26-46                      not more than 200 milligrams of codeine per 100

26-47    milliliters or per 100 grams;

26-48                      not more than 100 milligrams of dihydrocodeine

26-49    per 100 milliliters or per 100 grams;

26-50                      not more than 100 milligrams of ethylmorphine per

26-51    100 milliliters or per 100 grams;

26-52                      not more than 2.5 milligrams of diphenoxylate and

26-53    not less than 25 micrograms of atropine sulfate per dosage unit;

26-54                      not more than 15 milligrams of opium per 29.5729

26-55    milliliters or per 28.35 grams; and

26-56                      not more than 0.5 milligram of difenoxin and not

26-57    less than 25 micrograms of atropine sulfate per dosage unit;

26-58                (2)  unless specifically excepted or unless listed in

26-59    another penalty group, a material, compound, mixture, or

26-60    preparation containing the narcotic drug Buprenorphine or its

26-61    salts; and

26-62                (3)  unless specifically exempted or excluded or unless

26-63    listed in another penalty group, any material, compound, mixture,

26-64    or preparation that contains any quantity of pyrovalerone, a

26-65    substance [the following substances] having a stimulant effect on

26-66    the central nervous system, including its salts, isomers, and salts

26-67    of isomers[:]

26-68                      [Propylhexedrine; and]

26-69                      [Pyrovalerone].

 27-1          SECTION 19.  Subchapter D, Chapter 481, Health and Safety

 27-2    Code, is amended by adding Sections 481.1121 and 481.1151 to read

 27-3    as follows:

 27-4          Sec. 481.1121.  OFFENSE:  MANUFACTURE OR DELIVERY OF

 27-5    SUBSTANCE IN PENALTY GROUP 1-A.  (a)  Except as provided by this

 27-6    chapter, a person commits an offense if the person knowingly

 27-7    manufactures, delivers, or possesses with intent to manufacture or

 27-8    deliver a controlled substance listed in Penalty Group 1-A.

 27-9          (b)  An offense under this section is:

27-10                (1)  a state jail felony if the number of abuse units

27-11    of the controlled substance is fewer than 20;

27-12                (2)  a felony of the second degree if the number of

27-13    abuse units of the controlled substance is 20 or more but fewer

27-14    than 80;

27-15                (3)  a felony of the first degree if the number of

27-16    abuse units of the controlled substance is 80 or more but fewer

27-17    than 4,000; and

27-18                (4)  punishable by imprisonment in the institutional

27-19    division of the Texas Department of Criminal Justice for life or

27-20    for a term of not more than 99 years or less than 15 years and a

27-21    fine not to exceed $250,000, if the number of abuse units of the

27-22    controlled substance is 4,000 or more.

27-23          Sec. 481.1151.  OFFENSE:  POSSESSION OF SUBSTANCE IN PENALTY

27-24    GROUP 1-A.  (a)  Except as provided by this chapter, a person

27-25    commits an offense if the person knowingly possesses a controlled

27-26    substance listed in Penalty Group 1-A.

27-27          (b)  An offense under this section is:

27-28                (1)  a state jail felony if the number of abuse units

27-29    of the controlled substance is fewer than 20;

27-30                (2)  a felony of the third degree if the number of

27-31    abuse units of the controlled substance is 20 or more but fewer

27-32    than 80;

27-33                (3)  a felony of the second degree if the number of

27-34    abuse units of the controlled substance is 80 or more but fewer

27-35    than 4,000;

27-36                (4)  a felony of the first degree if the number of

27-37    abuse units of the controlled substance is 4,000 or more but fewer

27-38    than 8,000; and

27-39                (5)  punishable by imprisonment in the institutional

27-40    division of the Texas Department of Criminal Justice for life or

27-41    for a term of not more than 99 years or less than 15 years and a

27-42    fine not to exceed $250,000, if the number of abuse units of the

27-43    controlled substance is 8,000 or more.

27-44          SECTION 20.  Section 481.122(a), Health and Safety Code, is

27-45    amended to read as follows:

27-46          (a)  Except as provided [authorized] by this chapter, a

27-47    person commits an offense if the person knowingly [or

27-48    intentionally] delivers a controlled substance listed in Penalty

27-49    Group 1, 1-A, 2, or 3 or knowingly [or intentionally] delivers

27-50    marihuana and the person delivers the controlled substance or

27-51    marihuana to a person:

27-52                (1)  who is 17 years of age or younger;

27-53                (2)  who the actor knows or believes intends to deliver

27-54    the controlled substance or marihuana to a person 17 years of age

27-55    or younger;

27-56                (3)  who is enrolled in an elementary or secondary

27-57    school; or

27-58                (4)  who the actor knows or believes intends to deliver

27-59    the controlled substance or marihuana to a person who is enrolled

27-60    in an elementary or secondary school.

27-61          SECTION 21.  Section 481.123(a), Health and Safety Code, is

27-62    amended to read as follows:

27-63          (a)  For the purposes of this chapter, a controlled substance

27-64    analogue is considered to be a controlled substance listed in

27-65    Penalty Group 1 or 1-A if the analogue in whole or in part is

27-66    intended for human consumption and:

27-67                (1)  the chemical structure of the analogue is

27-68    substantially similar to the chemical structure of a controlled

27-69    substance listed in Schedule I or Penalty Group 1 or 1-A; or

 28-1                (2)  the analogue is specifically designed to produce

 28-2    an effect substantially similar to or greater than the effect of a

 28-3    controlled substance listed in Schedule I or Penalty Group 1 or

 28-4    1-A.

 28-5          SECTION 22.  Section 481.128, Health and Safety Code, is

 28-6    amended to read as follows:

 28-7          Sec. 481.128.  OFFENSE AND CIVIL PENALTY:  COMMERCIAL

 28-8    MATTERS.  (a)  A registrant or dispenser commits an offense if the

 28-9    registrant or dispenser knowingly [or intentionally]:

28-10                (1)  distributes, delivers, administers, or dispenses a

28-11    controlled substance in violation of Sections 481.070-481.075

28-12    [481.070-481.074];

28-13                (2)  manufactures a controlled substance not authorized

28-14    by the person's registration or distributes or dispenses a

28-15    controlled substance not authorized by the person's registration to

28-16    another registrant or other person;

28-17                (3)  refuses or fails to make, keep, or furnish a

28-18    record, report, notification, order form, statement, invoice, or

28-19    information required by this chapter;

28-20                (4)  prints, manufactures, possesses, or produces a

28-21    triplicate prescription form without the approval of the director

28-22    [Department of Public Safety];

28-23                (5)  delivers or possesses a counterfeit triplicate

28-24    prescription;

28-25                (6)  refuses an entry into a premise for an inspection

28-26    authorized by this chapter;

28-27                (7)  refuses or fails to return a triplicate

28-28    prescription form as required by Section 481.075(h); [or]

28-29                (8)  refuses or fails to make, keep, or furnish a

28-30    record, report, notification, order form, statement, invoice, or

28-31    information required by a rule adopted [before June 1, 1991,] by

28-32    the director; or

28-33                (9)  refuses or fails to maintain security required by

28-34    this chapter or a rule adopted under this chapter.

28-35          (b)  If the registrant or dispenser knowingly [or

28-36    intentionally] refuses or fails to make, keep, or furnish a record,

28-37    report, notification, order form, statement, invoice, or

28-38    information or maintain security required by a rule [or a rule

28-39    amendment] adopted [on or after June 1, 1991,] by the director, the

28-40    registrant or dispenser is liable to the state for a civil penalty

28-41    of not more than $5,000 for each act.

28-42          (c)  [If the registrant or dispenser negligently fails to

28-43    make, keep, or furnish a record, report, notification, order form,

28-44    statement, invoice, or information required by a rule or a rule

28-45    amendment adopted on or after June 1, 1991, by the director, the

28-46    registrant or dispenser is liable to the state for a civil penalty

28-47    of not more than $1,000 for each act.]

28-48          [(d)]  An offense under Subsection (a) is a state jail

28-49    felony.

28-50          (d) [(e)]  If a person [negligently] commits an act that

28-51    would otherwise be an offense under Subsection (a) except that it

28-52    was committed without the requisite culpable mental state, the

28-53    person is liable to the state for a civil penalty of not more

28-54    [less] than $1,000 [$5,000 or more than $10,000] for each act.

28-55          (e) [(f)]  A district attorney of the county where the act

28-56    occurred may file suit in district court in that county to collect

28-57    a civil penalty under this section, or the district attorney of

28-58    Travis County or the attorney general may file suit in district

28-59    court in Travis County to collect the penalty.

28-60          SECTION 23.  Subchapter D, Chapter 481, Health and Safety

28-61    Code, is amended by adding Sections 481.136-481.139 to read as

28-62    follows:

28-63          Sec. 481.136.  OFFENSE:  UNLAWFUL TRANSFER OR RECEIPT OF

28-64    CHEMICAL PRECURSOR.  (a)  A person commits an offense if the person

28-65    sells, transfers, furnishes, or receives a precursor substance

28-66    listed in Section 481.077(a) and the person:

28-67                (1)  does not hold a precursor transfer permit as

28-68    required by Section 481.078 at the time of the transaction;

28-69                (2)  does not comply with Section 481.077;

 29-1                (3)  knowingly makes a false statement in a report or

 29-2    record required by Section 481.077 or 481.078; or

 29-3                (4)  knowingly violates a rule adopted under Section

 29-4    481.077 or 481.078.

 29-5          (b)  An offense under this section is a state jail felony,

 29-6    unless it is shown on the trial of the offense that the defendant

 29-7    has been previously convicted of an offense under this section or

 29-8    Section 481.137, in which event the offense is a felony of the

 29-9    third degree.

29-10          Sec. 481.137.  OFFENSE:  TRANSFER OF PRECURSOR SUBSTANCE FOR

29-11    UNLAWFUL MANUFACTURE.  (a)  A person commits an offense if the

29-12    person sells, transfers, or otherwise furnishes a precursor

29-13    substance listed in Section 481.077(a) with the knowledge or intent

29-14    that the recipient will use the substance to unlawfully manufacture

29-15    a controlled substance or controlled substance analogue.

29-16          (b)  An offense under this section is a felony of the third

29-17    degree.

29-18          Sec. 481.138.  OFFENSE:  UNLAWFUL TRANSFER OR RECEIPT OF

29-19    CHEMICAL LABORATORY APPARATUS.  (a)  A person commits an offense if

29-20    the person sells, transfers, furnishes, or receives an apparatus

29-21    described by Section 481.080(a) and the person:

29-22                (1)  does not have an apparatus transfer permit as

29-23    required by Section 481.081 at the time of the transaction;

29-24                (2)  does not comply with Section 481.080;

29-25                (3)  knowingly makes a false statement in a report or

29-26    record required by Section 481.080 or 481.081; or

29-27                (4)  knowingly violates a rule adopted under Section

29-28    481.080 or 481.081.

29-29          (b)  An offense under this section is a state jail felony,

29-30    unless it is shown on the trial of the offense that the defendant

29-31    has been previously convicted of an offense under this section, in

29-32    which event the offense is a felony of the third degree.

29-33          Sec. 481.139.  OFFENSE:  TRANSFER OF CHEMICAL LABORATORY

29-34    APPARATUS FOR UNLAWFUL MANUFACTURE.  (a)  A person commits an

29-35    offense if the person sells, transfers, or otherwise furnishes an

29-36    apparatus described by Section 481.080(a) with the knowledge or

29-37    intent that the recipient will use the apparatus to unlawfully

29-38    manufacture a controlled substance or controlled substance

29-39    analogue.

29-40          (b)  An offense under Subsection (a) is a felony of the third

29-41    degree.

29-42          SECTION 24.  Section 481.160(e), Health and Safety Code, as

29-43    added by Chapter 285, Acts of the 72nd Legislature, Regular

29-44    Session, 1991, is relettered as Subsection (f) and amended to read

29-45    as follows:

29-46          (f) [(e)]  A law enforcement agency may petition a court to

29-47    require, as a condition of community supervision [probation] under

29-48    Article 42.12, Code of Criminal Procedure, a person to reimburse

29-49    the agency for the cost of the confiscation, analysis, storage, or

29-50    disposal of raw materials, controlled substances, chemical

29-51    precursors, drug paraphernalia, or other materials seized in

29-52    connection with an offense committed by the person under this

29-53    chapter.

29-54          SECTION 25.  Subchapter D, Chapter 12, Penal Code, is amended

29-55    by adding Section 12.48 to read as follows:

29-56          Sec. 12.48.  PENALTY IF CONTROLLED SUBSTANCE USED TO COMMIT

29-57    OFFENSE.  If the court makes an affirmative finding under Article

29-58    42.015, Code of Criminal Procedure, in the punishment phase of the

29-59    trial of an offense under Chapter 29, Chapter 31, or Title 5, other

29-60    than a first degree felony or a Class A misdemeanor, the punishment

29-61    for the offense is increased to the punishment prescribed for the

29-62    next highest category of offense.  If the offense is a Class A

29-63    misdemeanor, the minimum term of confinement for the offense is

29-64    increased to 180 days.

29-65          SECTION 26.  Chapter 42, Code of Criminal Procedure, is

29-66    amended by adding Article 42.015 to read as follows:

29-67          Art. 42.015.  FINDING THAT CONTROLLED SUBSTANCE USED TO

29-68    COMMIT OFFENSE.  In the punishment phase of the trial of an offense

29-69    under Chapter 29, Chapter 31, or Title 5, Penal Code, if the court

 30-1    determines beyond a reasonable doubt that the defendant

 30-2    administered or provided a controlled substance to the victim of

 30-3    the offense with the intent of facilitating the commission of the

 30-4    offense, the court shall make an affirmative finding of that fact

 30-5    and enter the affirmative finding in the judgment of that case.

 30-6          SECTION 27.  Section 15(d), Article 42.12, Code of Criminal

 30-7    Procedure, is amended to read as follows:

 30-8          (d)  A judge may impose as a condition of community

 30-9    supervision that a defendant submit at the beginning of the period

30-10    of community supervision to a term of confinement in a state jail

30-11    felony facility for a term of not less than 90 days or more than

30-12    180 days, or a term of not less than 90 days or more than one year

30-13    if the defendant is convicted of an offense punishable as a state

30-14    jail felony under Section 481.112, 481.1121, 481.113, or 481.120,

30-15    Health and Safety Code.  A judge may not require a defendant to

30-16    submit to both the term of confinement authorized by this

30-17    subsection and a term of confinement under Section 5 or 12 of this

30-18    article.  For the purposes of this subsection, a defendant

30-19    previously has been convicted of a felony regardless of whether the

30-20    sentence for the previous conviction was actually imposed or was

30-21    probated and suspended.

30-22          SECTION 28.  Sections 481.079 and 481.082, Health and Safety

30-23    Code, are repealed.

30-24          SECTION 29.  Not later than December 1, 1997, the

30-25    commissioner of public health shall file with the secretary of

30-26    state for publication in the Texas Register a list of substances

30-27    designated in Schedules I through V under Subchapter B, Chapter

30-28    481, Health and Safety Code, as amended by this Act.  The list

30-29    shall take effect January 1, 1998.  A schedule in effect

30-30    immediately before the effective date of this Act continues in

30-31    effect until January 1, 1998.

30-32          SECTION 30.  (a)  A change in law made by this Act applies

30-33    only to an offense committed on or after the effective date of this

30-34    Act.  For purposes of this section, an offense was committed before

30-35    the effective date of this Act if any element of the offense

30-36    occurred before the effective date.

30-37          (b)  An offense committed before the effective date of this

30-38    Act is covered by the law in effect when the offense was committed,

30-39    and the former law is continued in effect for this purpose.

30-40          SECTION 31.  (a)  Except as provided by Subsection (b) of

30-41    this section, this Act takes effect January 1, 1998.

30-42          (b)  Section 29 of this Act takes effect September 1, 1997.

30-43          SECTION 32.  The importance of this legislation and the

30-44    crowded condition of the calendars in both houses create an

30-45    emergency and an imperative public necessity that the

30-46    constitutional rule requiring bills to be read on three several

30-47    days in each house be suspended, and this rule is hereby suspended.

30-48                                 * * * * *