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U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

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The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER E - ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS
 
PART 510NEW ANIMAL DRUGS
 

Subpart A - General Provisions
   § 510.3 - Definitions and interpretations.
   § 510.4 - Biologics; products subject to license control.
   § 510.7 - Consignees of new animal drugs for use in the manufacture of animal feed.
   § 510.95 - [Reserved]

Subpart B - Specific Administrative Rulings and Decisions
   § 510.105 - Labeling of drugs for use in milk-producing animals.
   § 510.106 - Labeling of antibiotic and antibiotic-containing drugs intended for use in milk-producing animals.
   § 510.110 - Antibiotics used in food-producing animals.
   § 510.112 - Antibiotics used in veterinary medicine and for nonmedical purposes; required data.

Subpart C - Import Tolerances for Residues of Unapproved New Animal Drugs in Food
   § 510.201 - Scope.
   § 510.202 - Definitions.
   § 510.203 - Initiation of a proceeding to establish or amend an import tolerance.
   § 510.205 - Content and administration of a request.
   § 510.206 - Review of information supporting actions to establish or amend an import tolerance.
   § 510.207 - Disclosure of information submitted in a request.
   § 510.209 - Establishment, denial, or amendment of an import tolerance.
   § 510.210 - Revocation of an import tolerance.
   § 510.212 - Administrative reconsideration of action.
   § 510.213 - Administrative stay of action.

Subpart D - Records and Reports
   § 510.301 - Records 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.
   § 510.305 - Maintenance of copies of approved medicated feed mill licenses to manufacture animal feed bearing or containing new animal drugs.

Subpart E - Requirements for Specific New Animal Drugs
   § 510.410 - Corticosteroids for oral, injectable, and ophthalmic use in animals; warnings and labeling requirements.
   § 510.440 - Injectable iron preparations.
   § 510.455 - Requirements for free-choice medicated feeds.

Subpart F [Reserved]

Subpart G - Sponsors of Approved Applications
   § 510.600 - Names, addresses, and drug labeler codes of sponsors of approved applications.

Authority: 21 U.S.C. 321, 331, 351, 352, 353, 360b, 371, 379e.
Source: 40 FR 13807, Mar. 27, 1975, unless otherwise noted.

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