CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS (parts 500 to 590) > PART 522—IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS > 522.1150—Hydrochlorothiazide injection.

522.1150—Hydrochlorothiazide injection.

(a) Specifications. Each milliliter contains 25 milligrams of hydrochlorothiazide.
(b) Sponsor. See No. 050604 in § 510.600(c) of this chapter.
(c) Conditions of use— (1) Amount. 5 to 10 milliliters (125 to 250 milligrams) intravenously or intramuscularly once or twice a day. After onset of diuresis, treatment may be continued with an orally administered maintenance dose.
(2) Indications for use. For use in cattle as an aid in the treatment of postparturient udder edema. 1

Code of Federal Regulations

Footnote(s): 1 These conditions are NAS/NRC reviewed and deemed effective. Applications for these uses need not include effectiveness data as specified by § 514.111 of this chapter, but may require bioequivalency and safety information.
(3) Limitations. Animals should be regularly and carefully observed for early signs of fluid and electrolyte imbalance. Take appropriate countermeasures if this should occur. Milk taken from dairy animals during treatment and for 72 hours (6 milkings) after the latest treatment must not be used for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian. 1

Code of Federal Regulations

[43 FR 59058, Dec. 19, 1978, as amended at 62 FR 63271, Nov. 28, 1997]