FOOD AND DRUGS SUBCHAPTER VII-GENERAL AUTHORITY

§§ 371–379dd-2 · 58 sections

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails.

There are too many sections here to show them all on one page. 58 of them are listed on the subdivision pages linked above; open one to read them. Any sections that belong directly here are listed below.

Part A-General Administrative Provisions

Part D-Information and Education

Part E-Environmental Impact Review

Part B-Colors

Part C-Fees

Part F-National Uniformity for Nonprescription Drugs and Preemption for Labeling or Packaging of Cosmetics

Part G-Safety Reports

Part H-Serious Adverse Event Reports

Part I-Reagan-Udall Foundation for the Food and Drug Administration

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Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. Text of the U.S. Code 2024 Edition (govinfo), imported 2026-07-04. Amendments enacted after the 2024 Edition are not reflected. Read the official text ↗

Source: United States Code / CFR (uscode.house.gov, govinfo.gov) — U.S. federal law, public domain (17 U.S.C. § 105).

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