21 CFR 520.522
§ 520.522 Cyclosporine.
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 520.522, § 520.522 Cyclosporine, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87113
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Full text
(a) Specifications.
(1) Each cyclosporine capsule, USP (MODIFIED) contains 10, 25, 50, or 100 milligrams (mg) cyclosporine.
(2) Each milliliter of cyclosporine oral solution, USP (MODIFIED) contains 100 mg cyclosporine.
(b) Sponsors. See sponsors in § 510.600(c) of this chapter.
(1) No. 058198 for use of products described in paragraph (a) as in paragraph (d) of this section.
(2) No. 017033 for use of product described in paragraph (a)(1) as in paragraph (d)(1) of this section.
(3) No. 051311 for use of product described in paragraph (a)(2) of this section as in paragraph (d)(1) of this section.
(4) No. 013744 for use of product described in paragraph (a)(2) as in paragraph (d) of this section.
(c) [Reserved]
(d) Conditions of use—(1) Dogs. Use capsules described in paragraph (a)(1) of this section or solution as described in paragraph (a)(2) of this section as follows:
(i) Amount. Administer 5 mg per kilogram (mg/kg) of body weight given orally as a single daily dose for 30 days. Following this initial daily treatment period, the dosage may be tapered by decreasing the frequency of administration to every other day or two times a week, until a minimum frequency is reached which will maintain the desired therapeutic effect.
(ii) Indications for use. For the control of atopic dermatitis in dogs weighing at least 4 pounds.
(iii) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
(2) Cats. Use the solution described in paragraph (a)(2) of this section as follow:
(i) Amount. Administer 7 mg/kg of body weight orally as a single daily dose for a minimum of 4 to 6 weeks or until resolution of clinical signs. Following this initial daily treatment period, the dosage may be tapered by decreasing the frequency of administration to every other day or twice weekly to maintain the desired therapeutic effect.
(ii) Indications for use. For the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), miliary dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3 lbs (1.4 kg) in body weight.
(iii) Limitations. 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.