[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR522.518]

[Page 227]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 522--IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS--Table of Contents
 
Sec. 522.518  Cupric glycinate injection.

    (a) Specifications. Each milliliter (mL) of sterile aqueous 
suspension contains 200 milligrams of cupric glycinate (equivalent to 60 
milligrams of copper).
    (b) Sponsor. See No. 049185 in Sec. 510.600(c) of this chapter.
    (c) Conditions of use--(1) Amount. 200 milligrams (1 mL) for calves 
300 pounds and under; 400 milligrams (2 mL) for calves over 300 pounds 
and adult cattle.
    (2) Indications for use. For beef calves and beef cattle for the 
prevention of copper deficiency, or when labeled for veterinary 
prescription use, for the prevention and/or treatment of copper 
deficiency alone or in association with molybdenum toxicity.
    (3) Limitations. For subcutaneous use only; repeat dose in 3 months 
in young calves, in 6 months in cattle; discontinue use 30 days before 
treated animals are slaughtered for food use; Federal law restricts this 
drug to use by or on the order of a licensed veterinarian.

[46 FR 20159, Apr. 3, 1981, as amended at 52 FR 7832, Mar. 13, 1987; 62 
FR 28630, May 27, 1997]