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Regulations last checked for updates: Oct 30, 2025
Title 21 - Food and Drugs last revised: Sep 25, 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?
source:
81 FR 60212, Aug. 31, 2016, unless otherwise noted.
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