Part 207 — Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated Under a Biologics License Application, and Animal Drugs, and the National Drug Code
Subpart A — General
Subpart B — Registration
Subpart C — National Drug Code
Subpart D — Listing
- § 207.41— Who must list drugs and what drugs must they list?
- § 207.45— When, after initial registration of an establishment, must drug listing information be submitted?
- § 207.49— What listing information must a registrant submit for a drug it manufactures?
- § 207.53— What listing information must a registrant submit for a drug that it repacks or relabels?
- § 207.54— What listing information must a registrant submit for a drug that it salvages?
- § 207.55— What additional drug listing information may FDA require?
- § 207.57— What information must registrants submit when updating listing information and when?