U.S. Code of Federal Regulations

Regulations most recently checked for updates: Oct 30, 2025

All TitlesTitle 21Chapter IPart 329 - PART 329—NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
§ 329.100 - Postmarketing reporting of adverse drug events under section 760 of the Federal Food, Drug, and Cosmetic Act.
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