21 CFR 522.1920 - Prochlorperazine, isopropamide for injection.

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§ 522.1920 Prochlorperazine, isopropamide for injection.
(a) Specifications. Prochlorperazine, isopropamide for injection, veterinary, contains in each milliliter, 6 milligrams of prochlorperazine edisylate (equivalent to 4 milligrams prochlorperazine), and 0.38 milligrams of isopropamide iodide (equivalent to 0.28 milligrams of isopropamide) in buffered aqueous solution.
(b) Sponsor. See No. 000069 in § 510.600(c) of this chapter.
(c) Conditions of use.
(1) The drug is used in dogs and cats in which gastrointestinal disturbances are associated with emotional stress.
(2) Dosage is administered by subcutaneous injection twice daily as follows:
Weight of animal in pounds Dosage in Milliliters
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
Following the last injection, administer prochlorperazine and isopropamide sustained release capsules as indicated.
(3) For use only by or on the order of a licensed veterinarian.
[40 FR 13858, Mar. 27, 1975, as amended at 56 FR 50653, Oct. 8, 1991; 60 FR 55659, Nov. 2, 1995]

Title 21 published on 2013-04-01

The following are only the Rules published in the Federal Register after the published date of Title 21.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

  • 2014-04-15; vol. 79 # 72 - Tuesday, April 15, 2014
    1. 79 FR 21126 - New Animal Drugs; Ceftiofur Sodium; Gentamicin; Xylazine
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule; technical amendment.
      This rule is effective April 15, 2014.
      21 CFR Part 522

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

Title 21 published on 2013-04-01

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

  • 2014-04-15; vol. 79 # 72 - Tuesday, April 15, 2014
    1. 79 FR 21126 - New Animal Drugs; Ceftiofur Sodium; Gentamicin; Xylazine
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule; technical amendment.
      This rule is effective April 15, 2014.
      21 CFR Part 522