|
Home Page > Executive Branch > Code of Federal Regulations > Electronic Code of Federal Regulations
e-CFR Data is current as of February 4, 2010
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 510--NEW ANIMAL DRUGS
Subpart A--GENERAL PROVISIONS
|
| Definitions and interpretations. |
|
|
| Biologics; products subject to license control. |
|
|
| Consignees of new animal drugs for use in the manufacture of animal feed. |
|
Subpart B--SPECIFIC ADMINISTRATIVE RULINGS AND DECISIONS
|
| Labeling of drugs for use in milk-producing animals. |
|
|
| Labeling of antibiotic and antibiotic-containing drugs intended for use in milk-producing animals. |
|
|
| Antibiotics used in food-producing animals. |
|
|
| Antibiotics used in veterinary medicine and for nonmedical purposes; required data. |
|
Subpart C--[RESERVED]
Subpart D--RECORDS AND REPORTS
|
| 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. |
|
|
| 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
|
| Corticosteroids for oral, injectable, and ophthalmic use in animals; warnings and labeling requirements. |
|
|
| Injectable iron preparations. |
|
|
| Requirements for free-choice medicated feeds. |
|
Subpart F--[RESERVED]
Subpart G--SPONSORS OF APPROVED APPLICATIONS
|
| Names, addresses, and drug labeler codes of sponsors of approved applications. |
|
|
