 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
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 |
| § 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. |
| § 510.45 - Packaging requirements for drugs for animal use. |
| § 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 |
| § 510.300 - Records and reports concerning experience with new animal drugs for which an approved application is in effect. |
| § 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. |
| § 510.302 - Reporting forms. |
| § 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 - XXX |
| § 510.515 - Animal feeds bearing or containing new animal drugs subject to the provisions of section 512(n) of the act. |
| Subpart G - Sponsors of Approved Applications |
| § 510.600 - Names, addresses, and drug labeler codes of sponsors of approved applications. |