21 CFR 522.1920 - Prochlorperazine and isopropamide.

§ 522.1920 Prochlorperazine and isopropamide.

(a)Specifications. Each milliliter of solution contains prochlorperazine edisylate equivalent to 4 milligrams (mg) prochlorperazine and isopropamide iodide equivalent to 0.28 mg of isopropamide.

(b)Sponsor. See No. 054771 in § 510.600(c) of this chapter.

(c)Conditions of use -


(i) Dosage is administered by subcutaneous injection twice daily as follows:

Weight of animal in pounds Dosage in
Up to 4 0.25
5 to 14 0.5-1
15 to 30 2-3
30 to 45 3-4
45 to 60 4-5
Over 60 6

(ii) Following the last injection, administer prochlorperazine and isopropamide sustained release capsules as indicated.

(2)Indications for use. For use in dogs and cats in which gastrointestinal disturbances are associated with emotional stress.

(3)Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

[ 79 FR 16194, Mar. 25, 2014]

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

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United States Code
U.S. Code: Title 21 - FOOD AND DRUGS

Title 21 published on 19-May-2018 03:57

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR Part 522 after this date.

  • 2018-04-05; vol. 83 # 66 - Thursday, April 5, 2018
    1. 83 FR 14584 - New Animal Drugs; Approval of New Animal Drug Applications; Changes of Sponsorship; Change of a Sponsor's Name and Address
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule.
      This rule is effective April 5, 2018.
      21 CFR Parts 510, 520, 522, 526, and 558