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A BILL TO BE ENTITLED
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AN ACT
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relating to the scheduling of certain controlled substances in |
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response to certain actions by the United States Food and Drug |
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Administration with respect to those substances. |
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BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: |
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SECTION 1. Section 481.034, Health and Safety Code, is |
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amended by amending Subsections (a), (b), and (g) and adding |
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Subsection (g-1) to read as follows: |
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(a) The commissioner shall annually establish the schedules |
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of controlled substances. These annual schedules shall include the |
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complete list of all controlled substances from the previous |
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schedules and modifications in the federal schedules of controlled |
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substances as required by Subsection (g) or (g-1). Any further |
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additions to and deletions from these schedules, any rescheduling |
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of substances, and any other modifications made by the commissioner |
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to these schedules of controlled substances shall be made: |
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(1) in accordance with Section 481.035; |
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(2) in a manner consistent with this subchapter; and |
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(3) with approval of the executive commissioner. |
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(b) Except for alterations in schedules required by |
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Subsection (g) or (g-1), the commissioner may not make an |
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alteration in a schedule unless the commissioner holds a public |
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hearing on the matter in Austin and obtains approval from the |
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executive commissioner. |
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(g) Except as otherwise provided by this subsection or |
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Subsection (g-1), if a substance is designated, rescheduled, or |
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deleted as a controlled substance under federal law and notice of |
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that fact is given to the commissioner, the commissioner similarly |
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shall control the substance under this chapter. After the |
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expiration of a 30-day period beginning on the day after the date of |
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publication in the Federal Register of a final order designating a |
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substance as a controlled substance or rescheduling or deleting a |
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substance, the commissioner similarly shall designate, reschedule, |
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or delete the substance, unless the commissioner objects during the |
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period. If the commissioner objects, the commissioner shall |
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publish the reasons for the objection and give all interested |
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parties an opportunity to be heard. At the conclusion of the |
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hearing, the commissioner shall publish a decision, which is final |
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unless altered by statute. On publication of an objection by the |
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commissioner, control as to that particular substance under this |
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chapter is stayed until the commissioner publishes the |
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commissioner's decision. |
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(g-1) If a controlled substance listed in Schedule I is |
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approved by the United States Food and Drug Administration under |
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Section 505, Federal Food, Drug, and Cosmetic Act (21 U.S.C. |
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Section 355), the substance is subsequently deleted as a controlled |
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substance or rescheduled and placed on a lower schedule under |
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federal law, and notice of those facts is given to the commissioner, |
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as soon as practicable the commissioner similarly shall delete or |
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reschedule the substance under this chapter. |
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SECTION 2. The changes in law made by this Act apply only to |
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a controlled substance deleted as a controlled substance or |
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rescheduled and placed on a lower schedule under federal law on or |
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after the effective date of this Act. |
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SECTION 3. This Act takes effect September 1, 2023. |