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21 CFR 520.928

§ 520.928 Firocoxib tablets.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 520.928, § 520.928 Firocoxib tablets, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87159
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(a) Specifications. (1) Each chewable tablet contains 57 or 227 milligrams (mg) firocoxib. (2) Each tablet contains 57 mg firocoxib. (b) Sponsors. See sponsors in § 510.600(c) of this chapter as follows: (1) Nos. 000010, 013744, 055246, 055529, and 086101 for use of products described in paragraph (a)(1) as in paragraph (c)(1) of this section; and (2) Nos. 000010, 055246, and 086101 for use of the product described in paragraph (a)(2) of this section as in paragraph (c)(2) of this section. (c) Conditions of use—(1) Dogs—(i) Amount. 5 mg/kg (2.27 mg/lb) body weight. Administer once daily as needed for osteoarthritis and for 3 days as needed for postoperative pain and inflammation associated with soft-tissue and orthopedic surgery. Administer approximately 2 hours before soft tissue or orthopedic surgery. (ii) Indications for use. For the control of pain and inflammation associated with osteoarthritis; and for the control of postoperative pain and inflammation associated with soft-tissue and orthopedic surgery. (iii) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. (2) Horses—(i) Amount. Administer one 57-mg tablet to horses weighing 800 to 1,300 lb once daily for up to 14 days. (ii) Indications for use. For the control of pain and inflammation associated with osteoarthritis. (iii) Limitations. Do not use in horses intended for human consumption. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.