CFR 21, Parts 200 to 299, Food and Drugs, April 01, 2016 (Volume 4 of 9) by Office Of The Federal Register

CFR 21, Parts 200 to 299, Food and Drugs, April 01, 2016 (Volume 4 of 9) by Office Of The Federal Register

Code of Federal Regulations Title 21, Volume 4, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as:

- Code of Federal Regulations Title 21, Volume 4, April 1, 2016
- 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; REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMERCIAL DISTRIBUTION
- Part 208; MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
- Part 209; REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFECTS STATEMENT
- Part 210; CURENT GOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESING, PACKING, OR HOLDING OF DRUGS; GENERAL
- Part 211; CURENT GOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
- Part 212; CURENT GOD MANUFACTURING PRACTICE FOR POSITRON EMISION TOMOGRAPHY DRUGS
- Part 216; PHARMACY COMPOUNDING
- Part 225; CURENT GOD MANUFACTURING PRACTICE FOR MEDICATED FEDS
- Part 226; CURENT GOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
- Part 250; SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
- Part 290; CONTROLED DRUGS
- Part 299; DRUGS; OFICIAL NAMES AND ESTABLISHED NAMES