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/ Code of Federal Regulations / Title 21 / Chapter I — Food and Drug Administration, Department of Health and Human Services / Subchapter C — Drugs: General / Part 206 — Imprinting of Solid Oral Dosage Form Drug Products for Human Use

‹ Pt. 205Guidelines for State Licensing of Wholesale Prescription Drug Distributors Pt. 207Requirements 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 ›

Part 206 — Imprinting of Solid Oral Dosage Form Drug Products for Human Use

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§206.1 Scope.
§206.3 Definitions.
§206.7 Exemptions.
§206.10 Code imprint required.

‹ Pt. 205Guidelines for State Licensing of Wholesale Prescription Drug Distributors Pt. 207Requirements 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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