Schedule 2 Narcotics List

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Amendments 2012—Subsec. (c)., § 1152(b), added schedule I(c)(18) to (28)., § 1152(a), added schedule I(d).

Schedule 2 Narcotics List

Schedule 3 (III) Drugs. The drug has a potential for abuse less than the drugs in schedules 1 and 2. The drug has a currently accepted medical use in treatment in the United States. 2018 Schedules of Controlled Substances. Effective February 23, 2018. The republication was published in the February 2, 2018 issue of the Texas Register (43 TexReg 606) Amendment temporarily placing N-ethylpentylone into schedule I Effective November 23, 2018. The amendment was published in the November 2, 2018 issue of the Texas Register. Subject: Image Created Date: 3/9/2015 10:45:24 AM. This schedule II drug is marketed by Roxane Laboratories of Columbus, Ohio, under the trade name of Marinol (dronabinol). Marijuana on trial: is marijuana a dangerous drug or a valuable medicine? Add ephedrine and pseudoephedrine to the list of proscribed Schedule II drugs in state Health and Safety Code.

Schedule 2 Medication List Printable

Schedule 2 medication list printable

Schedule 3 Narcotics List

Added item (e) at end of schedule III. Amended schedule II(a)(4) generally. Prior to amendment, schedule II(a)(4) read as follows: “Coca leaves (except coca leaves and extracts of coca leaves from which cocaine, ecgonine, and derivatives of ecgonine or their salts have been removed); cocaine, its salts, optical and geometric isomers, and salts of isomers; and ecgonine, its derivatives, their salts, isomers, and salts of isomers.” amended schedule II(a)(4) generally. Prior to amendment, schedule II(a)(4) read as follows: “Coca leaves and any salt, compound, derivative, or preparation of coca leaves (including cocaine and ecgonine and their salts, isomers, derivatives, and salts of isomers and derivatives), and any salt, compound, derivative, or preparation thereof which is chemically equivalent or identical with any of these substances, except that the substances shall not include decocainized coca leaves or extraction of coca leaves, which extractions do not contain cocaine or ecgonine.” 1984—Subsec. (c)., § 507(c), in schedule II(a)(4) added applicability to cocaine and ecgonine and their salts, isomers, etc. (d)., § 509(b), struck out subsec. (d) which related to authority of Attorney General to except stimulants or depressants containing active medicinal ingredients.

Class 2 Narcotics List

“(1) In general.— The Congress finds that the abuse of illicit gamma hydroxybutyric acid is an imminent hazard to the public safety. Accordingly, the Attorney General, notwithstanding sections 201(a), 201(b), 201(c), and 202 of the Act [–(c), 812], shall issue, not later than 60 days after the date of the enactment of this Act [ Feb. 18, 2000], a final order that schedules such drug (together with its salts, isomers, and salts of isomers) in the same schedule under section 202(c) of the Controlled Substances Act as would apply to a scheduling of a substance by the Attorney General under section 201(h)(1) of such Act (relating to imminent hazards to the public safety), except as follows. For purposes of any requirements that relate to the physical security of registered and registered distributors, the final order shall treat such drug, when the drug is manufactured, distributed, or possessed in accordance with an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act [] (whether the exemption involved is authorized before, on, or after the date of the enactment of this Act [ Feb. 18, 2000]), as being in the same schedule as that recommended by the Secretary of Health and Human Services for the drug when the drug is the subject of an authorized investigational new drug application (relating to such section 505(i)). The recommendation referred to in the preceding sentence is contained in the first paragraph of the letter transmitted on May 19, 1999, by such Secretary (acting through the Assistant Secretary for Health) to the Attorney General (acting through the Deputy Administrator of the Drug Enforcement Administration), which letter was in response to the letter transmitted by the Attorney General (acting through such Deputy Administrator) on September 16, 1997. In publishing the final order in the Federal Register, the Attorney General shall publish a copy of the letter that was transmitted by the Secretary of Health and Human Services.

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