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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 D - Drugs for Human Use |
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Part 329 - Nonprescription Human Drug Products Subject to Section 760 of the Federal Food, Drug, and Cosmetic Act |
Part 329 - Nonprescription Human Drug Products Subject to Section 760 of the Federal Food, Drug, and Cosmetic Act
| § 329.100 - Postmarketing reporting of adverse drug events under section 760 of the Federal Food, Drug, and Cosmetic Act. |
| Subpart A - Derivatives Designated as Habit Forming |
| § 329.1 - Habit-forming drugs which are chemical derivatives of substances specified in section 502(d) of the Federal Food, Drug, and Cosmetic Act. |
| Subpart B - Labeling |
| § 329.10 - Labeling requirements for habit-forming drugs. |
| Subpart C - Exemptions |
| § 329.20 - Exemption of certain habit-forming drugs from prescription requirements. |