 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter C - Drugs: General |
|
|
Part 201 - Labeling |
|
|
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. |