21 CFR Part 329 - PART 329—NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT

CFR

§ 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.