HHS - 21 CFR PART 510
NEW ANIMAL DRUGS
active, Most Current
| Organization: | HHS |
| Publication Date: | 1 April 2015 |
| Status: | active |
| Page Count: | 11 |
scope:
General Provisions
Definitions and interpretations.
As used in this part:
(a) The term act means the Federal Food, Drug, and Cosmetic Act, as amended (secs. 201-902, 52 Stat. 1040 et seq., as amended; 21 U.S.C. 321-392).
(b) Department means the Department of Health and Human Services.
(c) Secretary means the Secretary of Health and Human Services.
(d) Commissioner means the Commissioner of Food and Drugs.
(e) Person means individuals, partnerships, corporations, and associations.
(f) The definitions and interpretations of terms contained in section 201 of the act shall be applicable to such terms when used in the regulations in this part.
Document History
April 1, 2022
NEW ANIMAL DRUGS
This subpart applies to tolerances for residues of new animal drugs not approved or conditionally approved for use in the United States, but lawfully used in another country and present in imported,...
21 CFR PART 510
April 1, 2015
NEW ANIMAL DRUGS
General Provisions
Definitions and interpretations.
As used in this part:
(a) The term act means the Federal Food, Drug, and Cosmetic Act, as amended (secs. 201–902, 52 Stat. 1040 et seq., as...