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§ 207.55 What additional drug listing information may FDA require?

21 CFR 207.55

Citation21 CFR 207.55
CorpusDaily eCFR
Displayed edition2026-09-16
Last updated2026-09-16

§ 207.55 What additional drug listing information may FDA require?

For a particular listed drug, upon our request, the registrant must briefly state the basis for its belief that the drug is not subject to section 505 or 512 of the Federal Food, Drug, and Cosmetic Act or section 351 of the Public Health Service Act.