ATROPINE SULFATE injection, solution

Atropine Sulfate by

Drug Labeling and Warnings

Atropine Sulfate by is a Animal medication manufactured, distributed, or labeled by Vedco, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

NDC 50989-075-12

ATROPINE SULFATE
Injection 1/120 Grain

STERILE MULTIPLE DOSE VIAL

NET CONTENTS: 100 mL

VEDCO

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.

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 & ADMINISTRATION

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.

WARNINGS

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

STORAGE AND HANDLING

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

Rev. 3/08
Distributed By
VEDCO, INC

St. Joseph, MO 64507

TAKE TIME OBSERVE LABEL DIRECTIONS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ATROPINE SULFATE 
atropine sulfate injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 50989-075
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	0.54 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50989-075-12	100 mL in 1 VIAL, MULTI-DOSE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/01/2008

Labeler - Vedco, Inc (021634266)