Federal (United States) · Regulations
Subpart D
6 sections
6 sections
- 21 C.F.R. § 207.41Who must list drugs and what drugs must they list?
- 21 C.F.R. § 207.49What listing information must a registrant submit for a drug it manufactures?
- 21 C.F.R. § 207.53What listing information must a registrant submit for a drug that it repacks or relabels?
- 21 C.F.R. § 207.54What listing information must a registrant submit for a drug that it salvages?
- 21 C.F.R. § 207.55What additional drug listing information may FDA require?
- 21 C.F.R. § 207.57What information must registrants submit when updating listing information and when?