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

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