Part 200 - General

Part 201 - Labeling

Part 202 - Prescription Drug Advertising

Part 203 - Prescription Drug Marketing

Part 205 - Guidelines for State Licensing of Wholesale Prescription Drug Distributors

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

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

Part 208 - Medication Guides for Prescription Drug Products

Part 209 - Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement

Part 210 - Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General

Part 211 - Current Good Manufacturing Practice for Finished Pharmaceuticals

Part 212 - Current Good Manufacturing Practice for Positron Emission Tomography Drugs

Part 216 - Human Drug Compounding

Part 225 - Current Good Manufacturing Practice for Medicated Feeds

Part 226 - Current Good Manufacturing Practice for Type a Medicated Articles

Part 250 - Special Requirements for Specific Human Drugs

Part 251 - Section 804 Importation Program

Part 290 - Controlled Drugs

Part 299 - Drugs; Official Names and Established Names