Subpart D. 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?