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
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Updated February 1, 2017
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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)