ATROPINE SULFATE- atropine sulfate injection, solution 
MWI

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 Injection

NDC 13985-354-04
 VETone


ATROPINE SULFATE
Injection 1/120 Grain

Sterile Multiple Dose Vial

Keep out of reach of children.

For veterinary use only.

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

 V1 510221                           Net Contents: 100 mL

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.

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

Rev. 02/14

Manufactured for: MWI
Boise, ID 83705

(888) 694-8381

www.VetOne.net

TAKE TIME OBSERVE LABEL DIRECTIONS

Lot No./Exp. Date:

Atropine Sulfate Inj- MWI Label

ATROPINE SULFATE 
atropine sulfate injection, solution
Product Information
Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:13985-354
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:13985-354-04100 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/200812/20/2022
Labeler - MWI (019926120)

Revised: 12/2022
 
MWI