Home/CFR/Title 21/Part 510
FEDERAL · 21 CFR

Part 510 — New Animal Drugs

24 sections · Title 21: Food and Drugs

§ 510.3Definitions and interpretations.
§ 510.4Biologics; products subject to license control.
§ 510.7Consignees of new animal drugs for use in the manufacture of animal feed.
§ 510.95§ 510.95 [Reserved]
§ 510.105Labeling of drugs for use in milk-producing animals.
§ 510.106Labeling of antibiotic and antibiotic-containing drugs intended for use in milk-producing animals.
§ 510.110Antibiotics used in food-producing animals.
§ 510.112Antibiotics used in veterinary medicine and for nonmedical purposes; required data.
§ 510.201Scope.
§ 510.202Definitions.
§ 510.203Initiation of a proceeding to establish or amend an import tolerance.
§ 510.205Content and administration of a request.
§ 510.206Review of information supporting actions to establish or amend an import tolerance.
§ 510.207Disclosure of information submitted in a request.
§ 510.209Establishment, denial, or amendment of an import tolerance.
§ 510.210Revocation of an import tolerance.
§ 510.212Administrative reconsideration of action.
§ 510.213Administrative stay of action.
§ 510.301Records and reports concerning experience with animal feeds bearing or containing new animal drugs for which an approved medicated feed mill license application is in effect.
§ 510.305Maintenance of copies of approved medicated feed mill licenses to manufacture animal feed bearing or containing new animal drugs.
§ 510.410Corticosteroids for oral, injectable, and ophthalmic use in animals; warnings and labeling requirements.
§ 510.440Injectable iron preparations.
§ 510.455Requirements for free-choice medicated feeds.
§ 510.600Names, addresses, and drug labeler codes of sponsors of approved applications.