21 CFR Subchapter C - DRUGS: GENERAL

  1. PART 200 - GENERAL (§§ 200.5 - 200.200)
  2. PART 201 - LABELING (§§ 201.1 - 201.328)
  3. PART 202 - PRESCRIPTION DRUG ADVERTISING (§ 202.1)
  4. PART 203 - PRESCRIPTION DRUG MARKETING (§§ 203.1 - 203.70)
  5. PART 205 - GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS (§§ 205.1 - 205.50)
  6. PART 206 - IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE (§§ 206.1 - 206.10)
  7. 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 (§§ 207.1 - 207.81)
  8. PART 208 - MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS (§§ 208.1 - 208.26)
  9. PART 209 - REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT (§§ 209.1 - 209.11)
  10. PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL (§§ 210.1 - 210.3)
  11. PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS (§§ 211.1 - 211.208)
  12. PART 212 - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS (§§ 212.1 - 212.110)
  13. PART 216 - HUMAN DRUG COMPOUNDING (§§ 216.23 - 216.24)
  14. PART 225 - CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS (§§ 225.1 - 225.202)
  15. PART 226 - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES (§§ 226.1 - 226.115)
  16. PART 250 - SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS (§§ 250.11 - 250.250)
  17. PART 290 - CONTROLLED DRUGS (§§ 290.1 - 290.10)
  18. PART 299 - DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES (§§ 299.3 - 299.5)