21 CFR Part 207 - 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?