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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Subpart D - Listing |
| § 207.40 - Establishment registration and drug listing requirements for foreign establishments. |
| § 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? |