21 CFR 522.144 - Arsenamide sodium aqueous injection.

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There are 12 Updates appearing in the Federal Register for 21 CFR 522. View below or at eCFR (GPOAccess)
§ 522.144 Arsenamide sodium aqueous injection.
(a) Chemical name. [[(p-Carbamoylphenyl) arsylene]dithio diacetic acid, sodium salt.
(b) Specifications. The drug is a sterile aqueous solution and each milliliter contains 10.0 milligrams of arsenamide sodium.
(c) Sponsor. See No. 050604 in § 510.600(c) of this chapter.
(d) Conditions of use.
(1) For the treatment and prevention of canine heartworm disease caused by Dirofilaria immitis.
(2) It is administered intravenously at 0.1 milliliter per pound of body weight (1.0 milliliter for every 10 pounds) twice a day for 2 days. For dogs in poor condition, particularly those with evidence of reduced liver function, a more conservative dosage schedule of 0.1 milliliter per pound of body weight daily for 15 days is recommended.
(3) Restricted to use only by or on the order of a licensed veterinarian.
[40 FR 13858, Mar. 27, 1975, as amended at 43 FR 27785, June 27, 1978; 45 FR 56798, Aug. 26, 1980; 55 FR 26683, June 29, 1990]

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