Atravet 10 mg Injectable (Canada)
This page contains information on Atravet 10 mg Injectable for veterinary use.The information provided typically includes the following:
- Atravet 10 mg Injectable Indications
- Warnings and cautions for Atravet 10 mg Injectable
- Direction and dosage information for Atravet 10 mg Injectable
Atravet 10 Mg Injectable
This treatment applies to the following species:Acepromazine Maleate Injection, Usp
Sterile
DIN 00053023
Veterinary Use Only
Description
Tranquilizer
ATRAVET depresses the action of the central nervous system, suppressing spontaneous motor activity and producing prolonged muscle relaxation.
The toxicity of ATRAVET is extremely low; no harmful effects on renal or hepatic function, or on hemopoietic activity have been found.
Active Ingredient per mL: Acepromazine maleate, USP 10 mg
Preservative: Benzyl alcohol 1% w/v
Atravet 10 mg Injectable Indications
For use in cattle, sheep, swine, goats and horses as an aid in tranquilizing animals:
a. Before loading
b. To facilitate restraint
c. To control hyperexcitability
d. As a pre-anesthetic agent in major and minor surgery
In colts - As an aid in breaking colts
In bulls and cows - To tranquilize animals for artificial insemination procedures
For use in dogs and cats as an aid in tranquilizing animals:
a. To facilitate restraint
b. As an aid in the control of hyperexcitability, vomiting, licking and scratching
c. As a pre-anesthetic agent in major and minor surgery
d. As an aid in breeding high strung bitches
Atravet 10 mg Injectable Dosage And Administration
Sheep And Goats
Sedation: Administer 0.05 mg to 0.1 mg per kg IMCattle
Sedation: 0.01 to 0.02 mg per kg IV or 0.03 to 0.1 mg per kg IMSedation prior to local anesthesia: 0.1 mg per kg IM
Swine
Sedation: Administer 0.01 mg to 0.2 mg per kg IV or IMDogs
Sedation: 0.025 to 0.2 mg per kg IV to a maximum dose of 3 mg IV or 0.1 to 0.25 mg per kg IM or SCPre-Anesthetic: 0.03 mg to 0.2 mg per kg IV, IM or SC with a maximum dose of 3 mg IV
Cats
Sedation: 0.05 mg to 0.11 mg per kg IV, IM or SC with a maximum dose of 1 mg IVHorses
Pre-anesthetic: 0.02 to 0.05 mg per kg IVTranquilization: 0.04 mg to 0.1 mg per kg IM
Dosages may be repeated in 10 hours.
As a preloading dose for cattle, sheep, goats, horses and swine, administer 25 mg/454 kg IV or 75 mg/454 kg IM one hour before loading.
Contraindications
Phenothiazine derivatives are contraindicated in animals being treated with organophosphates, succinylcholine or other cholinesterase inhibitors. Contraindicated in animals with hypovolemia or shock.
Epinephrine is contraindicated in the treatment of acepromazine maleate overdosage.
Atravet 10 mg Injectable Cautions
In horses, paralysis of the retractor penis muscle has been associated with the use of phenothiazine-derivative tranquilizers. This risk should be duly considered prior to the administration of acepromazine maleate to male horses (castrated and uncastrated). Use lower doses and use with caution when administering to animals with hepatic dysfunction, cardiac disease or general debilitation, due to possible prolongation of effect.
Warnings
Keep out of reach of children. Treated animals must not be slaughtered for use in food for at least 7 days after the latest treatment with this drug. Milk taken from treated animals during treatment and within 48 hours after the latest treatment must not be used as food. Do not use in horses that are to be slaughtered for use in food.
Storage
Store at room temperature 15° to 25°C
Supplied
ATRAVET 10 mg Injectable 50 mL DIN 00053023
Boehringer Ingelheim (canada) Ltd., 5180 South Service Road, Burlington, Ontario L7l 5h4
11760
A2400E
Nac No.
123006815180 SOUTH SERVICE ROAD, BURLINGTON, ON, L7L 5H4
| Customer Care No.: | 800-567-1885 | |
| Technical Services No.: | 1-877-565-5501 | |
| Website: | www.boehringer-ingelheim.ca |
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Every effort has been made to ensure the accuracy of the Atravet 10 mg Injectable information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the Canadian product label or package insert. |


