Subpart D—Listing

1. CFR
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3. Title 21
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5. Chapter I
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7. Part 207
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9. Subpart D

Sections

Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.

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