Label: ATROPINE SULFATE injection, solution
- NDC Code(s): 58005-307-04
- Packager: Sparhawk Laboratories, Inc.
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 1, 2017
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- Official Label (Printer Friendly)
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Each mL contains:
Atropine Sulfate ..................... 15 mg
Sodium Chloride ..................... 9 mg
Benzyl Alcohol .......................... 1%
Water for Injection .................... q.s.
- STORAGE AND HANDLING
DOSAGE AND ADMINISTRATION;
Cattle: 20 mg per 100 lbs. of body weight
Horses: 6.5 mg per 100 lbs. of body weight
Sheep: 20 mg per 100 lbs. of body weight
The recommended average initial dose should be split, injecting one quarter (1/4) to one-third (1/3) slowly I.V. and the remainder I.M. or S.C. After symptoms appear to be under control, repeated maintenance doses should be administered at 3 to 6 hour intervals based on the individual response of the animal.
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
atropine sulfate injection, solution
Product Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:58005-307 Route of Administration INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I) ATROPINE SULFATE 15 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58005-307-04 100 mL in 1 VIAL Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/1997 Labeler - Sparhawk Laboratories, Inc. (147979082)