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A BILL TO BE ENTITLED
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AN ACT
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relating to the addition of Salvia divinorum and its derivatives  | 
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and extracts to Penalty Group 3 of the Texas Controlled Substances  | 
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Act. | 
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       BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: | 
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       SECTION 1.  Section 481.104(a), Health and Safety Code, is  | 
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amended to read as follows: | 
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       (a)  Penalty Group 3 consists of: | 
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             (1)  a material, compound, mixture, or preparation that  | 
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contains any quantity of the following substances having a  | 
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potential for abuse associated with a stimulant effect on the  | 
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central nervous system: | 
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                   Methylphenidate and its salts; and | 
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                   Phenmetrazine and its salts; | 
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             (2)  a material, compound, mixture, or preparation that  | 
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contains any quantity of the following substances having a  | 
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potential for abuse associated with a depressant effect on the  | 
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central nervous system: | 
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                   a substance that contains any quantity of a  | 
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derivative of barbituric acid, or any salt of a derivative of  | 
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barbituric acid not otherwise described by this subsection; | 
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                   a compound, mixture, or preparation containing  | 
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amobarbital, secobarbital, pentobarbital, or any salt of any of  | 
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these, and one or more active medicinal ingredients that are not  | 
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listed in any penalty group; | 
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                   a suppository dosage form containing amobarbital,  | 
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secobarbital, pentobarbital, or any salt of any of these drugs, and  | 
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approved by the United States Food and Drug Administration for  | 
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marketing only as a suppository; | 
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                   Alprazolam; | 
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                   Amobarbital; | 
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                   Bromazepam; | 
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                   Camazepam; | 
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                   Chlordiazepoxide; | 
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                   Chlorhexadol; | 
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                   Clobazam; | 
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                   Clonazepam; | 
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                   Clorazepate; | 
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                   Clotiazepam; | 
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                   Cloxazolam; | 
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                   Delorazepam; | 
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                   Diazepam; | 
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                   Estazolam; | 
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                   Ethyl loflazepate; | 
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                   Fludiazepam; | 
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                   Flurazepam; | 
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                   Glutethimide; | 
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                   Halazepam; | 
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                   Haloxzolam; | 
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                   Ketazolam; | 
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                   Loprazolam; | 
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                   Lorazepam; | 
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                   Lormetazepam; | 
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                   Lysergic acid, including its salts, isomers, and  | 
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salts of isomers; | 
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                   Lysergic acid amide, including its salts,  | 
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isomers, and salts of isomers; | 
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                   Mebutamate; | 
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                   Medazepam; | 
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                   Methyprylon; | 
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                   Midazolam; | 
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                   Nimetazepam; | 
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                   Nitrazepam; | 
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                   Nordiazepam; | 
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                   Oxazepam; | 
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                   Oxazolam; | 
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                   Pentazocine, its salts, derivatives, or compounds  | 
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or mixtures thereof; | 
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                   Pentobarbital; | 
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                   Pinazepam; | 
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                   Prazepam; | 
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                   Quazepam; | 
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                   Secobarbital; | 
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                   Sulfondiethylmethane; | 
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                   Sulfonethylmethane; | 
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                   Sulfonmethane; | 
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                   Temazepam; | 
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                   Tetrazepam; | 
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                   Tiletamine and zolazepam in combination, and its  | 
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salts. (some trade or other names for a tiletamine-zolazepam  | 
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combination product: Telazol, for tiletamine:  | 
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2-(ethylamino)-2-(2-thienyl)-cyclohexanone, and for zolazepam:  | 
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4-(2-fluorophenyl)-6,  | 
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8-dihydro-1,3,8,-trimethylpyrazolo-[3,4-e](1,4)-d  | 
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diazepin-7(1H)-one, flupyrazapon); | 
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                   Triazolam; | 
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                   Zaleplon; and | 
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                   Zolpidem; | 
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             (3)  Nalorphine; | 
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             (4)  a material, compound, mixture, or preparation  | 
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containing limited quantities of the following narcotic drugs, or  | 
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any of their salts: | 
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                   not more than 1.8 grams of codeine, or any of its  | 
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salts, per 100 milliliters or not more than 90 milligrams per dosage  | 
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unit, with an equal or greater quantity of an isoquinoline alkaloid  | 
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of opium; | 
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                   not more than 1.8 grams of codeine, or any of its  | 
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salts, per 100 milliliters or not more than 90 milligrams per dosage  | 
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unit, with one or more active, nonnarcotic ingredients in  | 
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recognized therapeutic amounts; | 
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                   not more than 300 milligrams of dihydrocodeinone  | 
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(hydrocodone), or any of its salts, per 100 milliliters or not more  | 
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than 15 milligrams per dosage unit, with a fourfold or greater  | 
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quantity of an isoquinoline alkaloid of opium; | 
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                   not more than 300 milligrams of dihydrocodeinone  | 
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(hydrocodone), or any of its salts, per 100 milliliters or not more  | 
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than 15 milligrams per dosage unit, with one or more active,  | 
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nonnarcotic ingredients in recognized therapeutic amounts; | 
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                   not more than 1.8 grams of dihydrocodeine, or any  | 
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of its salts, per 100 milliliters or not more than 90 milligrams per  | 
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dosage unit, with one or more active, nonnarcotic ingredients in  | 
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recognized therapeutic amounts; | 
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                   not more than 300 milligrams of ethylmorphine, or  | 
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any of its salts, per 100 milliliters or not more than 15 milligrams  | 
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per dosage unit, with one or more active, nonnarcotic ingredients  | 
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in recognized therapeutic amounts; | 
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                   not more than 500 milligrams of opium per 100  | 
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milliliters or per 100 grams, or not more than 25 milligrams per  | 
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dosage unit, with one or more active, nonnarcotic ingredients in  | 
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recognized therapeutic amounts; | 
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                   not more than 50 milligrams of morphine, or any of  | 
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its salts, per 100 milliliters or per 100 grams with one or more  | 
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active, nonnarcotic ingredients in recognized therapeutic amounts;   | 
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and | 
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                   not more than 1 milligram of difenoxin and not  | 
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less than 25 micrograms of atropine sulfate per dosage unit; | 
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             (5)  a material, compound, mixture, or preparation that  | 
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contains any quantity of the following substances: | 
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                   Barbital; | 
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                   Chloral betaine; | 
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                   Chloral hydrate; | 
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                   Ethchlorvynol; | 
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                   Ethinamate; | 
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                   Meprobamate; | 
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                   Methohexital; | 
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                   Methylphenobarbital (Mephobarbital); | 
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                   Paraldehyde; | 
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                   Petrichloral; and | 
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                   Phenobarbital; | 
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             (6)  Peyote, unless unharvested and growing in its  | 
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natural state, meaning all parts of the plant classified  | 
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botanically as Lophophora, whether growing or not, the seeds of the  | 
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plant, an extract from a part of the plant, and every compound,  | 
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manufacture, salt, derivative, mixture, or preparation of the  | 
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plant, its seeds, or extracts; | 
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             (7)  unless listed in another penalty group, a  | 
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material, compound, mixture, or preparation that contains any  | 
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quantity of the following substances having a stimulant effect on  | 
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the central nervous system, including the substance's salts,  | 
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optical, position, or geometric isomers, and salts of the  | 
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substance's isomers, if the existence of the salts, isomers, and  | 
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salts of isomers is possible within the specific chemical  | 
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designation: | 
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                   Benzphetamine; | 
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                   Cathine [(+)-norpseudoephedrine]; | 
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                   Chlorphentermine; | 
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                   Clortermine; | 
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                   Diethylpropion; | 
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                   Fencamfamin; | 
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                   Fenfluramine; | 
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                   Fenproporex; | 
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                   Mazindol; | 
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                   Mefenorex; | 
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                   Modafinil; | 
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                   Pemoline (including organometallic complexes and  | 
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their chelates); | 
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                   Phendimetrazine; | 
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                   Phentermine; | 
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                   Pipradrol; | 
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                   Sibutramine; and | 
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                   SPA [(-)-1-dimethylamino-1,2-diphenylethane]; | 
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             (8)  unless specifically excepted or unless listed in  | 
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another penalty group, a material, compound, mixture, or  | 
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preparation that contains any quantity of the following substance,  | 
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including its salts: | 
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                   Dextropropoxyphene (Alpha-(+)-  | 
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4-dimethylamino-1,2-diphenyl-3-methyl-2-propionoxybutane); [and] | 
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             (9)  an anabolic steroid or any substance that is  | 
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chemically or pharmacologically related to testosterone, other  | 
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than an estrogen, progestin, or corticosteroid, and promotes muscle  | 
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growth, including: | 
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                   Boldenone; | 
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                   Chlorotestosterone (4-chlortestosterone); | 
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                   Clostebol; | 
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                   Dehydrochlormethyltestosterone; | 
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                   Dihydrotestosterone (4-dihydrotestosterone); | 
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                   Drostanolone; | 
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                   Ethylestrenol; | 
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                   Fluoxymesterone; | 
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                   Formebulone; | 
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                   Mesterolone; | 
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                   Methandienone; | 
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                   Methandranone; | 
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                   Methandriol; | 
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                   Methandrostenolone; | 
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                   Methenolone; | 
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                   Methyltestosterone; | 
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                   Mibolerone; | 
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                   Nandrolone; | 
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                   Norethandrolone; | 
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                   Oxandrolone; | 
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                   Oxymesterone; | 
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                   Oxymetholone; | 
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                   Stanolone; | 
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                   Stanozolol; | 
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                   Testolactone; | 
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                   Testosterone; and | 
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                   Trenbolone; and | 
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             (10)  Salvia divinorum, unless unharvested and growing  | 
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in its natural state, meaning all parts of that plant, whether  | 
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growing or not, the seeds of that plant, an extract from a part of  | 
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that plant, and every compound, manufacture, salt, derivative,  | 
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mixture, or preparation of that plant, its seeds, or extracts,  | 
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including Salvinorin A. | 
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       SECTION 2.  This Act takes effect September 1, 2009. |