21 CFR Subchapter C - 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 213—XXX (§§ - )
  14. PART 216—HUMAN DRUG COMPOUNDING (§§ 216.23 - 216.24)
  15. PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS (§§ 225.1 - 225.202)
  16. PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES (§§ 226.1 - 226.115)
  17. PART 230—XXX (§§ - )
  18. PART 250—SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS (§§ 250.11 - 250.250)
  19. PART 251—SECTION 804 IMPORTATION PROGRAM (§§ 251.1 - 251.21)
  20. PART 290—CONTROLLED DRUGS (§§ 290.1 - 290.10)
  21. PART 299—DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES (§§ 299.3 - 299.5)