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Regulations last checked for updates: May 22, 2025

Title 21 - Food and Drugs last revised: May 19, 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.
authority: 21 U.S.C. 321,331,351,352,353,355,371,379aa
source: 79 FR 33089, June 10, 2014, unless otherwise noted.
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