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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Aug 28, 2025
All Titles
Title 21
Chapter I
Part 207
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?
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