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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 C - National Drug Code |
| § 207.20 - Who must register and submit a drug list. |
| § 207.22 - How and where to register and list drugs. |
| § 207.26 - Amendments to registration. |
| § 207.30 - Updating drug listing information. |
| § 207.31 - Additional drug listing information. |
| § 207.33 - What is the National Drug Code (NDC), how is it assigned, and what are its requirements? |
| § 207.35 - What changes require a new NDC? |
| § 207.37 - What restrictions pertain to the use of the NDC? |
| § 207.39 - Misbranding by reference to registration or to registration number. |