Listing

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Drugs: General
  6. Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated Under a Biologics License Application, and Animal Drugs, and the National Drug Code
  7. Listing

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Section
207.41

Who must list drugs and what drugs must they list?

Section
207.45

When, after initial registration of an establishment, must drug listing information be submitted?

Section
207.49

What listing information must a registrant submit for a drug it manufactures?

Section
207.53

What listing information must a registrant submit for a drug that it repacks or relabels?

Section
207.54

What listing information must a registrant submit for a drug that it salvages?

Section
207.55

What additional drug listing information may FDA require?

Section
207.57

What information must registrants submit when updating listing information and when?