DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES

GENERAL

LABELING

PRESCRIPTION DRUG ADVERTISING

PRESCRIPTION DRUG MARKETING

GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS

IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE

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

MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS

REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT

HUMAN DRUG COMPOUNDING

CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL

CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS

CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS

CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS

CONTROLLED DRUGS