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Code of Federal Regulations

Subpart D

Listing

207.41Who must list drugs and what drugs must they list?207.45When, after initial registration of an establishment, must drug listing information be submitted?207.49What listing information must a registrant submit for a drug it manufactures?207.53What listing information must a registrant submit for a drug that it repacks or relabels?207.54What listing information must a registrant submit for a drug that it salvages?207.55What additional drug listing information may FDA require?207.57What information must registrants submit when updating listing information and when?