21 CFR 530.2 - Purpose.

§ 530.2 Purpose.

The purpose of this part is to establish conditions for extralabel use or intended extralabel use in animals by or on the lawful order of licensed veterinarians of

Food and Drug Administration
approved new animal drugs and approved new human drugs. Such use is limited to treatment modalities when the health of an animal is threatened or suffering or death may result from failure to treat. This section implements the
Animal Medicinal Drug Use Clarification Act of 1994
(the AMDUCA) ( Pub. L. 103-396).

Title 21 published on 09-Nov-2018 03:23

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR Part 530 after this date.

  • 2012-01-06; vol. 77 # 4 - Friday, January 6, 2012
    1. 77 FR 735 - New Animal Drugs; Cephalosporin Drugs; Extralabel Animal Drug Use; Order of Prohibition
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule.
      This rule becomes effective April 5, 2012. Submit either electronic or written comments on this document by March 6, 2012.
      21 CFR Part 530