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Code of Federal Regulations, Title 21 Food Drugs 200 - 299, Revised as of April 1, 2025

by Office of the Federal Register (U S )

A federal regulatory reference for food and drug law

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AlbakiReads Editorial

A federal regulatory reference for food and drug law

This volume covers Title 21, Parts 200–299 of the Code of Federal Regulations, in a revision dated April 1, 2025. Its scope brings together regulations promulgated by the FDA, DEA, and Office of the National Drug Control Agency across food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. The annual revision date makes the edition’s coverage period an important detail for reference use; the book presents regulations as of the date stated in its title.

Good fit for readers who enjoy

  • Legal professionals seeking a reference to Title 21, Parts 200–299.
  • Readers researching federal regulation of food, drugs, medical devices, cosmetics, or controlled substances.

Themes

Federal regulationsFood and drug lawHealth and safetyControlled substances

Based on publisher information and book metadata.

Book overview

Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.
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