Code of Federal Regulations Title 21, Volume 4, April 1, 2015

21 CFR Parts 200-299 covers prescription drug products for human use, manufacturing, labeling, processing, and packing practices, official drug names, and more.

Code of Federal Regulations Title 21, Volume 4, April 1, 2015

Containing parts Parts 200 to 299

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; REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION

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 216; PHARMACY COMPOUNDING

Part 225; CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS

Part 226; CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

Part 250; SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS

Part 290; CONTROLLED DRUGS

Part 299; DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES