21 CFR 520.2002

§ 520.2002 Propiopromazine.

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

Cite this

Citation: 21 CFR 520.2002, § 520.2002 Propiopromazine, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87294
Permanent ID: ys:prov:87294@1
SHA-256: 4572a053d058c7938287d6497d6ec564a1230ee139f43270c9670b48c5d2bd33

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Full text

(a) Specifications. Each chewable tablet contains 10 or 20 milligrams of propiopromazine hydrochloride. (b) Sponsor. See No. 054771 in § 510.600(c) of this chapter. (c) Conditions of use in dogs—(1) Amount. Administer 0.5 to 2.0 milligrams per pound of body weight once or twice daily, depending upon the degree of tranquilization desired. (2) Indications for use. For oral administration as a tranquilizer. As an aid in handling difficult, excited, and unruly dogs, and in controlling excessive kennel barking, car sickness, and severe dermatitis. It is also indicated for use in minor surgery and prior to routine examinations, laboratory procedures, and diagnostic procedures. (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.