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Code of Federal Regulations

Subchapter C

Drugs: General

200General 201Labeling 202Prescription Drug Advertising 203Prescription Drug Marketing 205Guidelines for State Licensing of Wholesale Prescription Drug Distributors 206Imprinting of Solid Oral Dosage Form Drug Products for Human Use 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 208Medication Guides for Prescription Drug Products 209Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement 210Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General 211Current Good Manufacturing Practice for Finished Pharmaceuticals 212Current Good Manufacturing Practice for Positron Emission Tomography Drugs 213Current Good Manufacturing Practice for Medical Gases 216Human Drug Compounding 225Current Good Manufacturing Practice for Medicated Feeds 226Current Good Manufacturing Practice for Type a Medicated Articles 230Certification and Postmarketing Reporting for Designated Medical Gases 250Special Requirements for Specific Human Drugs 251Section 804 Importation Program 290Controlled Drugs 299Drugs; Official Names and Established Names