21 CFR Part 290 - CONTROLLED DRUGS | US Law | LII / Legal Information Institute

SUBPART A — General Provisions (§§ 290.1 - 290.10)
SUBPART B — [Reserved]
SUBPART C — Requirements for Specific Controlled Drugs [Reserved]

Authority:

Source:

40 FR 14040, Mar. 27, 1975, unless otherwise noted.

Title 21 published on 2015-04-01.

No entries appear in the Federal Register after this date, for 21 CFR Part 290.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.

United States Code

U.S. Code: Title 21 - FOOD AND DRUGS

§ 352 - Misbranded drugs and devices

§ 353 - Exemptions and consideration for certain drugs, devices, and biological products

§ 355 - New drugs

§ 371 - Regulations and hearings