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[A2]

 

Electronic Code of Federal Regulations

e-CFR data is current as of November 19, 2019

Title 21 → Chapter I → Subchapter E → Part 510

TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS

PART 510—NEW ANIMAL DRUGS

rule

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]
rule

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.
rule

Subpart C—[RESERVED]

rule

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.
rule

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.
rule

Subpart F—[RESERVED]

rule

Subpart G—SPONSORS OF APPROVED APPLICATIONS

§510.600
Names, addresses, and drug labeler codes of sponsors of approved applications.

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