{"product_id":"code-of-federal-regulations-title-21-volume-4-april-1-2015-paperback","title":"Code of Federal Regulations Title 21, Volume 4, April 1, 2015 - Paperback","description":"\u003cdiv\u003e\u003cp style=\"text-align: right;\"\u003e\u003ca href=\"https:\/\/reportcopyrightinfringement.com\/\" target=\"_blank\" rel=\"nofollow\"\u003e\u003cb\u003eReport copyright infringement\u003c\/b\u003e\u003c\/a\u003e\u003c\/p\u003e\u003c\/div\u003e\u003cp\u003eby \u003cb\u003eOffice of the Federal Register\u003c\/b\u003e (Created by)\u003c\/p\u003e\u003cp\u003e21 CFR Parts 200-299 covers prescription drug products for human use, manufacturing, labeling, processing, and packing practices, official drug names, and more.\u003cbr\u003e\u003cbr\u003eCode of Federal Regulations Title 21, Volume 4, April 1, 2015\u003cbr\u003e\u003cbr\u003eContaining parts Parts 200 to 299\u003cbr\u003e\u003cbr\u003ePart 200; GENERAL\u003cbr\u003ePart 201; LABELING\u003cbr\u003ePart 202; PRESCRIPTION DRUG ADVERTISING\u003cbr\u003ePart 203; PRESCRIPTION DRUG MARKETING\u003cbr\u003ePart 205; GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS\u003cbr\u003ePart 206; IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE\u003cbr\u003ePart 207; REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION\u003cbr\u003ePart 208; MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS\u003cbr\u003ePart 209; REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT\u003cbr\u003ePart 210; CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL\u003cbr\u003ePart 211; CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS\u003cbr\u003ePart 212; CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS\u003cbr\u003ePart 216; PHARMACY COMPOUNDING\u003cbr\u003ePart 225; CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS\u003cbr\u003ePart 226; CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES\u003cbr\u003ePart 250; SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS\u003cbr\u003ePart 290; CONTROLLED DRUGS\u003cbr\u003ePart 299; DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES\u003c\/p\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003eNumber of Pages:\u003c\/strong\u003e 250\u003c\/div\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003eDimensions:\u003c\/strong\u003e 0.53 x 9.21 x 6.14 IN\u003c\/div\u003e\n            \u003cdiv\u003e\n\u003cstrong\u003ePublication Date:\u003c\/strong\u003e March 01, 2016\u003c\/div\u003e\n            ","brand":"BooksCloud","offers":[{"title":"Default Title","offer_id":52698481590579,"sku":"9781354240199","price":69.91,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0300\/5595\/6612\/files\/Do7eubYCyM9781354240199.webp?v=1763171683","url":"https:\/\/www.vysn.com\/products\/code-of-federal-regulations-title-21-volume-4-april-1-2015-paperback","provider":"VYSN","version":"1.0","type":"link"}