Federal Food, Drug, and Cosmetic Act, 21 United States Code (U.S.C), §301 et seq.Â
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Part 70 - Color AdditivesÂ
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Part 71 - Color Additive PetitionsÂ
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Part 73 - Listing of Color Additives Exempt From CertificationÂ
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Part 74 - Listing of Color Additives Subject to CertificationÂ
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Part 80 - Color Additive CertificationÂ
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Part 81 - General Specifications & Restrictions for Provisional Color Additives for use in Foods, Drugs, & CosmeticsÂ
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Part 82 - Listing of Certified Provisionally Listed Colors and SpecificationsÂ
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Part 200 - GeneralÂ
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Part 201 - LabelingÂ
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Part 202 - Prescription Drug AdvertisingÂ
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Part 203 - Prescription Drug MarketingÂ
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Part 205 - Guidelines for State Licensing of Wholesale Prescription Drug DistributorsÂ
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Part 206 - Imprinting of Solid Oral Dosage Form Drug Products for Human UseÂ
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Part 207 - Registration of Producers of Drugs and Listing of Drugs in Commercial DistributionÂ
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Part 210 - Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; GeneralÂ
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Part 211 - Current Good Manufacturing Practice for Finished PharmaceuticalsÂ
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Part 216 - Pharmacy CompoundingÂ
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Part 225 - Current Good Manufacturing Practice for Medicated FeedsÂ
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Part 226 - Current Good Manufacturing Practice for Type A Medicated ArticlesÂ
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Part 250 - Special Requirements For Specific Human DrugsÂ
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Part 290 - Controlled DrugsÂ
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Part 299 - Drugs; Official & Established NamesÂ
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Part 300 - GeneralÂ
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Part 310 - New DrugsÂ
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Part 312 - Investigational New Drug ApplicationÂ
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Part 314 - Applications for FDA Approval to Market a New Drug or an Antibiotic DrugÂ
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Part 315 - Diagnostic RadiopharmaceuticalsÂ
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Part 316 - Orphan DrugsÂ
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Part 320 - Bioavailability and Bioequivalence RequirementsÂ
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Part 361 - Prescription Drugs for Human Use Generally Recognized as Safe, Effective, & Not Misbranded: Used In ResearchÂ
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Part 500 - GeneralÂ
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Part 510 - New Animal DrugsÂ
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Part 511 - New Animal Drugs for Investigational UseÂ
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Part 514 - New Animal Drug ApplicationsÂ
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Part 515 - Medicated Feed Mill LicenseÂ
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Part 520 - Oral Dosage Form New Animal DrugsÂ
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Part 522 - Implantation or Injectable Dosage Form New Animal DrugsÂ
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Part 524 - Opthalmic and Topical Dosage Form New Animal DrugsÂ
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Part 526 - Intramammary Dosage FormsÂ
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Part 529 - Certain Other Dosage Form New Animal DrugsÂ
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Part 530 - Extralabel Drug Use in AnimalsÂ
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Part 556 - Tolerances for Residues of New Animal Drugs in FoodÂ
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Part 558 - New Animal Drugs for Use in Animal FeedsÂ
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Part 589 - Substances Prohibited From Use in Animal Food or FeedÂ
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Part 600 - Biological Products: GeneralÂ
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Part 601 - LicensingÂ
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Part 610 - General Biological Products StandardsÂ
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Part 660 - Additional Standards for Diagnostic Substances for Laboratory TestsÂ
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Part 680 - Additional Standards for Miscellaneous ProductsÂ
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Part 1300 - DefinitionsÂ
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Part 1301 - Registration of Manufacturers, Distributors, & Dispensers of Controlled SubstancesÂ
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Part 1302 - Labeling & Packaging Requirements For Controlled SubstancesÂ
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Part 1304 - Records & Reports of RegistrantsÂ
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Part 1305 - Orders for Schedule I & II Controlled SubstancesÂ
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Part 1306 - PrescriptionsÂ
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Part 1307 - MiscellaneousÂ
U.S. Food and Drug AdministrationÂ