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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 208 — Medication Guides for Prescription Drug Products
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Pt. 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
Pt. 209
Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement
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Part 208 — Medication Guides for Prescription Drug Products
Search Part 208 full text →
Subpt. A
General Provisions
§§208.1 to 208.3
Subpt. B
General Requirements for a Medication Guide
§§208.20 to 208.26
‹
Pt. 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
Pt. 209
Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement
›
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