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Home Page > Executive Branch > Code of Federal Regulations > Electronic Code of Federal Regulations
e-CFR Data is current as of November 3, 2008
TITLE 21--Food and Drugs
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER C--DRUGS: GENERAL
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| PRESCRIPTION DRUG ADVERTISING
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| PRESCRIPTION DRUG MARKETING
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| GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
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| IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
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| REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION
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| MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
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| REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
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| CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
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| CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
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| CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
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| CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
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| SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
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| DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES
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February 27, 2007< !-- #EndDate -- >-->
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