Atropine Sulfate: Product Information

ATROPINE SULFATE — atropine sulfate injection, solution
Med-Pharmex, Inc

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.

NDC 54925-063-10
ATROPINE SULFATE
Sterile Multiple Dose Vial
Injection 1/120 Grain

Net Contents: 100 mL

KEEP OUT OF REACH OF CHILDREN

FOR ANIMAL USE ONLY

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

MED -PHARMEX INCORPORATED Pomona, CA 91767

For Intravenous, Intramuscular, or Subcutaneous Use
COMPOSITION: Each mL contains:
Atropine Sulfate ………………………. 0.54 mg
Sodium Chloride …………………………… 9 mg
Benzyl Alcohol (preservative)…………… 1.5%
Water for Injection …………………………. q.s.
pH adjusted with sulfuric acid when necessary.

DOSAGE AND ADMINISTRATION:
Dogs and Cats: Inject 1 mL for each 20 lbs. of body weight as a pre-anesthetic adjuvant, or to reduce salivation, bronchial secretions, or internal peristalsis associated with colic or diarrhea.
As an antidote for parasympathomimetic drugs, 1 mL for each 7.5 lbs. of body weight. It is suggested that 1/4 of the dosage be injected intravenous and the remainder intramuscular or subcutaneous.

WARNING: Poisonous alkaloid. Keep out of reach of children
Antidotes: warmth, emetics, cholinergics.

Store at room temperature between 15° and 30°C (59°- 86°F)

Rev. 4/08

Distributed By
MED-PHARMEX INCORPORATED
Pomona, CA 91767
TAKE TIME OBSERVE LABEL DIRECTIONS

Atropine Sulfate 100 mL
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ATROPINE SULFATE atropine sulfate injection, solution
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:54925-063
Route of Administration INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATROPINE SULFATE (ATROPINE) ATROPINE SULFATE 0.54 mg in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54925-063-10 100 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/01/2008
Labeler — Med-Pharmex, Inc (025353699)

Revised: 04/2008 Med-Pharmex, Inc

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