yourstate.us
21 CFR 520.666

§ 520.666 Dirlotapide.

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

Get this as JSONEmbed this
Cite this
Citation
21 CFR 520.666, § 520.666 Dirlotapide, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87137
Permanent ID
ys:prov:87137@1
SHA-256
22955087cad2da7407bc56bf37b98e80feeed10951b5a5ef95b606cef85654e0

The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.

Full text

(a) Specifications. Each milliliter (mL) of solution contains 5 milligrams (mg) dirlotapide. (b) Sponsor. See No. 054771 in § 510.600(c) of this chapter. (c) Conditions of use in dogs—(1) Amount. The initial dosage is 0.01 mL/kg (0.0045 mL/lb) body weight for the first 14 days. After the first 14 days of treatment, the dose volume is doubled to 0.02 mL/kg (0.009 mL/lb) body weight for the next 14 days (days 15 to 28 of treatment). Dogs should be weighed monthly and the dose volume adjusted every month, as necessary, to maintain a target percent weight loss until the desired weight is achieved. (2) Indications for use. For the management of obesity. (3) 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.