Subchap C — Drugs: General
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- Pt. 200 General §§200.5 to 200.200
- Pt. 201 Labeling §§201.1 to 201.328
- Pt. 202 Prescription Drug Advertising §202.1
- Pt. 203 Prescription Drug Marketing §§203.1 to 203.70
- Pt. 205 Guidelines for State Licensing of Wholesale Prescription Drug Distributors §§205.1 to 205.50
- Pt. 206 Imprinting of Solid Oral Dosage Form Drug Products for Human Use §§206.1 to 206.10
- 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 §§207.1 to 207.81
- Pt. 208 Medication Guides for Prescription Drug Products §§208.1 to 208.26
- Pt. 209 Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement §§209.1 to 209.11
- Pt. 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General §§210.1 to 210.3
- Pt. 211 Current Good Manufacturing Practice for Finished Pharmaceuticals §§211.1 to 211.208
- Pt. 212 Current Good Manufacturing Practice for Positron Emission Tomography Drugs §§212.1 to 212.110
- Pt. 213 Current Good Manufacturing Practice for Medical Gases §§213.1 to 213.208
- Pt. 216 Human Drug Compounding §§216.23 to 216.24
- Pt. 225 Current Good Manufacturing Practice for Medicated Feeds §§225.1 to 225.202
- Pt. 226 Current Good Manufacturing Practice for Type a Medicated Articles §§226.1 to 226.115
- Pt. 230 Certification and Postmarketing Reporting for Designated Medical Gases §§230.1 to 230.230
- Pt. 250 Special Requirements for Specific Human Drugs §§250.11 to 250.250
- Pt. 251 Section 804 Importation Program §§251.1 to 251.21
- Pt. 290 Controlled Drugs §§290.1 to 290.10
- Pt. 299 Drugs; Official Names and Established Names §§299.3 to 299.5