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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 226 - Current Good Manufacturing Practice for Type a Medicated Articles |
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Subpart E - Records and Reports |
| § 226.102 - Master-formula and batch-production records. |
| § 226.110 - Distribution records. |
| § 226.115 - Complaint files. |