21 CFR Subpart D
Listing
June 25, 2020
§
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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