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The Federal Analogue Act, 21 U.S.C. § 813, is a section of the United States Controlled Substances Act passed in 1986 which allows any chemical "substantially similar" to a controlled substance listed in Schedule I or II to be treated as if it were listed
A controlled substance analogue shall, to the extent intended for human consumption, be treated, for the purposes of any Federal law as a controlled substance in schedule I. The marketing, advertising, and labeling of the substance. The known efficacy or usefulness of the substance for the marketed, advertised, or labeled purpose.
The Controlled Substances Act (CSA) is the statute establishing federal U.S. drug policy under which the manufacture, importation, possession, use, and distribution of certain substances is regulated.
A controlled substance analogue shall, to the extent intended for human consumption, be treated, for the purposes of any Federal law as a controlled substance in schedule I.
9 paź 2019 · The CSA also applies to controlled substance analogues that are intended to mimic the effects of controlled substances and to certain listed chemicals —precursor chemicals commonly used to manufacture controlled substances.
In determining whether a controlled substance analogue was intended for human consumption under subsection (a), the following factors may be considered, along with any other relevant factors: (1) The marketing, advertising, and labeling of the substance.
The Controlled Substances Analogue Enforcement Act (CSA) of 1986 (section §802 (32) (A) and §813) defines a “controlled substance analogue” as a substance (i) whose chemical structure is substantially similar to the structure of a scheduled substance; (ii) whose effects are substantially similar to or greater than the effects of a ...
