21 CFR 522.2404 - Thialbarbitone sodium for injection.

§ 522.2404 Thialbarbitone sodium for injection.

(a)Specifications. Thialbarbitone sodium for injection when reconstituted with sterile distilled water provides 94 milligrams of thialbarbitone sodium per milliliter of solution.

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

(c)Conditions of use.

(1) The drug is administered as a general anesthetic in surgical procedures on dogs, cats, swine, sheep, cattle, and horses. The drug is used for procedures of relatively short duration. However, the period of anesthesia can be lengthened by slower initial injection and supplemental administration during surgery.

(2) It is administered intravenously. The drug is injected slowly to dogs, cats, cattle, sheep, and swine. For horses, it is recommended that a pre-anesthetic sedation be administered to the horse 30 minutes before the drug is administered. The drug is then injected rapidly and completely. The drug is used at the following dosage levels:

Species Weight of animal in pounds Dosage in milligrams per pound
Dog Over 50 14.1
Do 30-50 18.8
Do 10-30 23.5
Do Under 10 28.2
Cat 31.3-37.6
Horse 6.3-7.8
Cattle and swine 6.7-9.4
Calves and sheep 9.4-11.8

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

[ 40 FR 13858, Mar. 27, 1975, as amended at 79 FR 16196, 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