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21 CFR 522.1850

§ 522.1850 Polysulfated glycosaminoglycan.

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

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21 CFR 522.1850, § 522.1850 Polysulfated glycosaminoglycan, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87513
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(a) Specifications. (1) Each 1-milliliter (mL) ampule of solution contains 250 milligrams (mg) polysulfated glycosaminoglycan. (2) Each mL of solution packaged in 5-mL ampules or 20-, 30-, or 50-mL vials contains 100 mg polysulfated glycosaminoglycan. (b) Sponsor. See No. 010797 in § 510.600(c) of this chapter. (c) Special considerations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. (d) Conditions of use—(1) Horses—(i) Indications for use. For the treatment of noninfectious degenerative and/or traumatic joint dysfunction and associated lameness of the carpal and hock joints in horses. (ii) Amount—(A) Intra-articular use (carpal): 250 mg once a week for 5 weeks. (B) Intramuscular use (carpal and hock): 500 mg every 4 days for 28 days. (iii) Limitations. Do not use in horses intended for human consumption. (2) Dogs—(i) Indications for use. For control of signs associated with noninfectious degenerative and/or traumatic arthritis of canine synovial joints. (ii) Amount. 2 mg per pound of body weight by intramuscular injection twice weekly for up to 4 weeks (maximum of 8 injections).

Legislative history

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