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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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Part 211 - Current Good Manufacturing Practice for Finished Pharmaceuticals |
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Subpart G - Packaging and Labeling Control |
| § 211.122 - Materials examination and usage criteria. |
| § 211.125 - Labeling issuance. |
| § 211.130 - Packaging and labeling operations. |
| § 211.132 - Tamper-evident packaging requirements for over-the-counter (OTC) human drug products. |
| § 211.134 - Drug product inspection. |
| § 211.137 - Expiration dating. |