21 C.F.R. · Food and Drugs
21 C.F.R. § 25.33

Animal drugs.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 25.33 — Animal drugs.

§ 25.33 Animal drugs. The classes of actions listed in this section are categorically excluded and, therefore, ordinarily do not require the preparation of an EA or an EIS: (a) Action on an NADA, abbreviated application, request for determination of eligibility for indexing, a supplement to such applications, or a modification of an index listing, if the action does not increase the use of the drug. Actions to which this categorical exclusion applies may include: (1) An animal drug to be marketed under the same conditions of approval as a previously approved animal drug; (2) A combination of previously approved animal drugs; (3) A new premix or other formulation of a previously approved animal drug; (4) Changes specified in § 514.8(b)(3), (b)(4), or (c)(3) of this chapter; (5) A change of sponsor; or (6) A previously approved animal drug to be contained in medicated feed blocks under § 510.455 of this chapter or as a liquid feed supplement under § 558.5 of this chapter. (b) [Reserved] (c) Action on an NADA, abbreviated application, request for determination of eligibility for indexing, a supplement to such applications, or a modification of an index listing, for substances that occur naturally in the environment when the action does not alter significantly the concentration or distribution of the substance, its metabolites, or degradation products in the environment. (d) Action on an NADA, abbreviated application, request for determination of eligibility for indexing, a supplement to such applications, or a modification of an index listing, for: (1) Drugs intended for use in nonfood animals; (2) Anesthetics, both local and general, that are individually administered; (3) Nonsystemic topical and ophthalmic animal drugs; (4) Drugs for minor species, including wildlife and endangered species, when the drug has been previously approved for use in another or the same species where similar animal management practices are used; and (5) Drugs intended for use under prescription or veterinarian's order for therapeutic use in terrestrial species. (e) Action on an INAD. (f) Action on an application submitted under section 512(m) of the act. (g) Withdrawal of approval of an NADA or an abbreviated NADA or removal of a new animal drug from the index. (h) Withdrawal of approval of a food additive petition that reduces or eliminates animal feed uses of a food additive. [62 FR 40592, July 29, 1997, as amended at 71 FR 74782, Dec. 13, 2006; 72 FR 69119, Dec. 6, 2007; 85 FR 72907, Nov. 16, 2020]

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
Root-LD Entity Data
◈ Machine-Readable Provenance Record Root-LD v1.0 · boisestandard.org
Federation ID
BS-CFR21-SEC-CC7C3D
Entity Class
REGULATION / FEDERAL-CFR-SECTION
Domain Signature
boisestandard.org
Citation
21 C.F.R. § 25.33
Corpus
CFR — Code of Federal Regulations
Status
✓ ACTIVE
Source
PRIMARY-SOURCE
Source Verified
✓ TRUE
Content Hash
7496a7f1c1a0e921...
Semantic Edges
Pending — corpus passes queued
The regulatory text of 21 C.F.R. § 25.33 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
Navigate Corpus — Title 21 C.F.R.
◈ Provenance
boisestandard.org United States Law CFR Title 21 21 C.F.R. § 25.33