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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 429 - DRUGS COMPOSED WHOLLY OR PARTLY OF INSULIN |
| Subpart A - General Provisions |
| § 429.3 - Definitions and interpretations. |
| Subpart B - Packaging and Labeling |
| § 429.10 - Packaging. |
| § 429.11 - Labeling. |
| § 429.12 - Distinguishing colors on packages. |
| Subpart C - Product Standards |
| § 429.25 - Standards of quality and purity for protamine. |
| § 429.26 - Standards of quality and purity for globin hydrochloride. |
| Subpart D - Tests and Methods |
| § 429.30 - Tests and methods of assay. |
| Subpart E - Certification |
| § 429.40 - Requests for certification; samples; storage; approvals preliminary to certification. |
| § 429.41 - Certifications. |
| § 429.45 - Conditions on the effectiveness of certificates. |
| § 429.47 - Authority to refuse certification service. |
| Subpart F - Administrative Procedures |
| § 429.50 - Hearing procedure. |
| § 429.55 - Fees. |
| Subpart G - Records |
| § 429.60 - Records of distribution. |