Code of Federal Regulations · Subchapter
Subchapter C — Drugs: General
21 C.F.R. subch. C
- 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 213 Current Good Manufacturing Practice For Medical Gases
- 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 230 Certification And Postmarketing Reporting For Designated Medical Gases
- 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