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Code of Federal Regulations (Last Updated: October 10, 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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Part 201 - Labeling |
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Subpart D - Exemptions From Adequate Directions for Use |
| § 201.100 - Prescription drugs for human use. |
| § 201.105 - Veterinary drugs. |
| § 201.115 - New drugs or new animal drugs. |
| § 201.116 - Drugs having commonly known directions. |
| § 201.117 - Inactive ingredients. |
| § 201.119 - In vitro diagnostic products. |
| § 201.120 - Prescription chemicals and other prescription components. |
| § 201.122 - Drugs for processing, repacking, or manufacturing. |
| § 201.125 - Drugs for use in teaching, law enforcement, research, and analysis. |
| § 201.127 - Drugs; expiration of exemptions. |
| § 201.128 - Meaning of “intended uses”. |
| § 201.129 - Drugs; exemption for radioactive drugs for research use. |