Code of Federal Regulations > Title 21 > Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

U.S. Code of Federal Regulations

Regulations most recently checked for updates: May 21, 2022

Part 200 [§ 200.5 - § 200.200] - GENERAL

Part 201 [§ 201.1 - § 201.328] - LABELING

Part 202 [§ 202.1 - § 202.1] - PRESCRIPTION DRUG ADVERTISING

Part 203 [§ 203.1 - § 203.70] - PRESCRIPTION DRUG MARKETING

Part 205 [§ 205.1 - § 205.50] - GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS

Part 206 [§ 206.1 - § 206.10] - IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE

Part 207 [§ 207.1 - § 207.81] - 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 [§ 208.1 - § 208.26] - MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS

Part 209 [§ 209.1 - § 209.11] - REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT

Part 210 [§ 210.1 - § 210.3] - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL

Part 211 [§ 211.1 - § 211.208] - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

Part 212 [§ 212.1 - § 212.110] - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS

Part 216 [§ 216.23 - § 216.24] - HUMAN DRUG COMPOUNDING

Part 225 [§ 225.1 - § 225.202] - CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS

Part 226 [§ 226.1 - § 226.115] - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

Part 250 [§ 250.11 - § 250.250] - SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS

Part 251 [§ 251.1 - § 251.21] - SECTION 804 IMPORTATION PROGRAM

Part 290 [§ 290.1 - § 290.10] - CONTROLLED DRUGS

Part 299 [§ 299.3 - § 299.5] - DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES