ATROPINE SULFATE- atropine sulfate injection, solution 
Vedco, 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.

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Atropine Sulfate 

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 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. 3/08
Distributed By
VEDCO, INC

St. Joseph, MO 64507

TAKE TIME OBSERVE LABEL DIRECTIONS

Atropine Sulfate Inj VEDCO label

ATROPINE SULFATE 
atropine sulfate injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:50989-075
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I) ATROPINE SULFATE 0.54 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50989-075-12100 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/01/200812/22/2022
Labeler - Vedco, Inc (021634266)

Revised: 12/2022
 
Vedco, Inc