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Code of Federal Regulations
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Title 21
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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 207 — Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated under a Biologics License Application, and Animal Drugs, and the National Drug Code
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Pt. 206
Imprinting of Solid Oral Dosage Form Drug Products for Human Use
Pt. 208
Medication Guides for Prescription Drug Products
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Part 207 — Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated under a Biologics License Application, and Animal Drugs, and the National Drug Code
Search Part 207 full text →
Subpt. A
General
§§207.1 to 207.13
Subpt. B
Registration
§§207.17 to 207.29
Subpt. C
National Drug Code
§§207.33 to 207.37
Subpt. D
Listing
§§207.41 to 207.57
Subpt. E
Electronic Format for Registration and Listing
§§207.61 to 207.65
Subpt. F
Miscellaneous
§§207.69 to 207.81
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Pt. 206
Imprinting of Solid Oral Dosage Form Drug Products for Human Use
Pt. 208
Medication Guides for Prescription Drug Products
›
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