ATROPINE SULFATE description, usages, side effects, indications, overdosage, supplying and lots more!

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ATROPINE SULFATE

Sparhawk Laboratories, Inc

ATROPINE SULFATE 1/120 INJECTABLE SOLUTION


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

INDICATIONS

For use in Dogs and Cats as an antidote in the treatment of organophosphate insecticide poisoning; to reduce salivation, bronchial secretions or intestinal peristalsis associated with colic or diarrhea, and as a preanesthetic adjuvant.

DOSAGE AND ADMINISTRATION:

Dogs and Cats:  Inject intravenously, intramuscularly, or subcutaneously, 1 mL for each 20 lbs of body weight as a preanesthetic adjuvant, or to reudce salivation, bronchial secretions, or intestinal peristalsis associated with colic or diarrhea. 

As an antidote for parasympathomimetic drugs, inject 1 mL for each 5 lbs of body weight administered to effect and repeat as necessary.  It is suggested that 1/4 of the dosage be injected intravenously and the remainder intramuscularly or subcutaneously.

WARNING

Poisonous alkaloid.

Antidotes:  Warmth, Emetics, Cholinergics

COMPOSITION

Each mL of sterile solution contains:


Atropine Sulfate  ............................  0.54 mg
Sodium Chloride .................................  9 mg
Benzyl Alcohol  ..................................  1.5%
Water for Injection  ................................  QS

Store at controlled room temperature between 15o and 30oC (59o-86oF)

PROTECT FROM LIGHT

TAKE TIME OBSERVE LABEL DIRECTIONS

ATROPINE SULFATE 1/120 INJECTABLE SOLUTION

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.

NET CONTENTS

ATROPINE SULFATE

ATROPINE SULFATE

ATROPINE SULFATE INJECTION, SOLUTION

Product Information

Product Type Prescription animal drug label Item Code (Source) NDC:58005-354
Route of Administration INTRAVENOUS DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
atropine sulfate ATROPINE 0.54 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58005-354-04 100 in 1 VIAL

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1997-06-01


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