Code of Federal Regulations · Subpart

Subpart D — Listing

21 C.F.R. pt. 207, subpt. D

• § 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?