Code Of Federal Regulations Title 21, Volume 4, April 1, 2015 [Paperback]

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, 2015Containing parts Parts 200 to 299Part 200; GENERALPart 201; LABELINGPart 202; PRESCRIPTION DRUG ADVERTISINGPart 203; PRESCRIPTION DRUG MARKETINGPart 205; GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORSPart 206; IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USEPart 207; REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTIONPart 208; MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTSPart 209; REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENTPart 210; CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERALPart 211; CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALSPart 212; CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGSPart 216; PHARMACY COMPOUNDINGPart 225; CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDSPart 226; CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLESPart 250; SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGSPart 290; CONTROLLED DRUGSPart 299; DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES