CFR 21, Parts 200 to 299, Food and Drugs, April 01, 2017 (Volume 4 of 9)

Code of Federal Regulations Title 21, Volume 4, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 4, April 1, 2017 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 200 to 299, Food and Drugs This volume contains 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; 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; 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; HUMAN DRUG 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