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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 314 - Applications for FDA Approval to Market a New Drug |
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Subpart G - Miscellaneous Provisions |
| § 314.410 - Imports and exports of new drugs. |
| § 314.420 - Drug master files. |
| § 314.430 - Availability for public disclosure of data and information in an application or abbreviated application. |
| § 314.440 - Addresses for applications and abbreviated applications. |
| § 314.445 - Guidance documents. |