ACEPROMAZINE MALEATE

Manufacturer
Covetrus North America | ZYVET ANIMAL HEALTH INC.
Effective date
2024-11-08
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:43:53

Label at a glance#

ProductACEPROMAZINE MALEATE
Active ingredientACEPROMAZINE MALEATE
Label structure18 sections

Dosage and administration

Dogs: 0.25-1.0 mg/lb of body weight. Dosage may be repeated as required.

Label contents#

Full prescribing information#

Acepromazine Maleate Tablets

SPL UNCLASSIFIED SECTION

For use in dogs only.

Caution:

SPL UNCLASSIFIED SECTION

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

Description:

SPL UNCLASSIFIED SECTION

Acepromazine maleate, a potent neuroleptic agent with a low order of toxicity, is of particular value in the tranquilization of dogs. Its rapid action and lack of hypnotic effect are added advantages.

Chemistry:

SPL UNCLASSIFIED SECTION

2-acetyl-10-(3-dimethylaminopropyl) phenothiazine hydrogen maleate.

Acepromazine Maleate

Chemistry:
Chemistry:

Mode of Action:

SPL UNCLASSIFIED SECTION

Acepromazine maleate has a depressant effect on the central nervous system and therefore causes sedation, muscular relaxation and a reduction in spontaneous activity. It acts rapidly,exerting a prompt and pronounced calming effect. It is an effective preanesthetic agent and lowers the dosage requirement of general anesthetics.

Indications:

SPL UNCLASSIFIED SECTION

As an aid in tranquilization and as a preanesthetic agent in dogs.

Acepromazine Maleate Tablets can be used as an aid in controlling intractable animals during examination, treatment, grooming, x-ray and minor surgical procedures.

Dosage and Administration:

SPL UNCLASSIFIED SECTION

Dogs: 0.25-1.0 mg/lb of body weight. Dosage may be repeated as required.

Animal Safety:

SPL UNCLASSIFIED SECTION

Acute and chronic toxicity studies have shown a very low order of toxicity for acepromazine maleate.

A safety study using elevated dosages of acepromazine maleate demonstrated no adverse reactions even when administered at three times the upper limit of the recommended daily dosage (3.0 mg/lb body weight). The clinical observation for this high dosage was mild depression which disappeared in most dogs 24 hours after termination of dosing.

The only occurrence of adverse reaction during numerous clinical trials was a very mild respiratory distress (reverse sneeze) which was transient in nature and had no effect on the desired action of the drug.

Contraindications:

SPL UNCLASSIFIED SECTION

Phenothiazines may potentiate the toxicity of organophosphates. Therefore, do not use acepromazine maleate to control tremors associated with organic phosphate poisoning.

Do not use in conjunction with organophosphorus vermifuges or ectoparasiticides, including flea collars.

Do not use with procaine hydrochloride.

Warning:

SPL UNCLASSIFIED SECTION

Do not use in animals intended for human consumption.

Keep Acepromazine Maleate Tablets in a secure location out of reach of dogs, cats, and other animals to prevent accidental ingestion or overdose.

Precautions:

SPL UNCLASSIFIED SECTION

Tranquilizers are potent central nervous system depressants, and they can cause marked sedation with suppression of the sympathetic nervous system. Tranquilizers can produce prolonged depression or motor restlessness when given in excessive amounts or when given to sensitive animals.

Tranquilizers are additive in action to the actions of other depressants and will potentiate general anesthesia. Tranquilizers should be administered in smaller doses and with greater care during general anesthesia and also to animals exhibiting symptoms of stress, debilitation, cardiac disease, sympathetic blockade, hypovolemia or shock. Acepromazine, like other phenothiazine derivatives, is detoxified in the liver; therefore, it should be used with caution on animals with a previous history of liver dysfunction or leukopenia.

Epinephrine is contraindicated for treatment of acute hypotension produced by phenothiazine-derivative tranquilizers since further depression of blood pressure can occur.

Phenothiazines should be used with caution when followed by epidural anesthetic procedures because they may potentiate the arterial hypotensive effects of local anesthetics.

Adverse Reactions:

SPL UNCLASSIFIED SECTION

A few rare but serious occurrences of idiosyncratic reactions to acepromazine may occur in dogs following oral or parenteral administration. These potentially serious adverse reactions include behavioral disorders in dogs such as aggression, biting/chewing, and nervousness.

To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Covetrus® North America at (855) 724-3461.

For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or www.fda.gov/reportanimalae

Storage:

SPL UNCLASSIFIED SECTION

Store at 20° - 25°C (68° - 77°F). Excursions permitted to 40°C (104°F).

How Supplied:

SPL UNCLASSIFIED SECTION

Acepromazine Maleate Tablets are available in 10 and 25 mg quarter-scored tablets and are supplied in bottles containing 100 and 500 tablets.

NDC 11695-7034-1 – 10 mg – 100 tablets

NDC 11695-7034-2 – 10 mg – 500 tablets

NDC 11695-7033-1 – 25 mg – 100 tablets

NDC 11695-7033-2 – 25 mg – 500 tablets

Approved by FDA under ANADA # 200-757

Questions?

(855) 724-3461

Distributed by:

Covetrus® North America

400 Metro Place North

Dublin, OH 43017

covetrus.com

Made in India

CC-AcepromazineTabPI-01

REV: 0624

© 2024 Covetrus, Inc. All rights reserved.

Principal Display Panel - Bottle Label, 10 mg – 100 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Covetrus

NDC:11695-7034-1

Acepromazine Maleate Tablets

10 mg

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

Approved by FDA under ANADA # 200-757

Net Contents:

100 tablets

10 mg 100 tab
10 mg 100 tab

Principal Display Panel - Bottle Label, 10 mg - 500 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Covetrus

NDC:11695-7034-2

Acepromazine Maleate Tablets

10 mg

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

Approved by FDA under ANADA # 200-757

Net Contents:

500 tablets

10 mg 500 tab
10 mg 500 tab

Principal Display Panel - Bottle Label, 25 mg - 100 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Covetrus

NDC:11695-7033-1

Acepromazine Maleate Tablets

25 mg

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

Approved by FDA under ANADA # 200-757

Net Contents:

100 tablets

25 mg 100 tab
25 mg 100 tab

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Covetrus

NDC:11695-7033-2

Acepromazine Maleate Tablets

25 mg

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

Approved by FDA under ANADA # 200-757

Net Contents:

500 tablets

25 mg 500 tab
25 mg 500 tab

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1116448acepromazine maleate 10 MG Oral TabletPSN1
1116450acepromazine maleate 25 MG Oral TabletPSN1
1116448acepromazine maleate 10 MG Oral TabletSCD1
1116450acepromazine maleate 25 MG Oral TabletSCD1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11695-7033-1ACEPROMAZINE MALEATE100 in 1 BOTTLETABLET1001
11695-7033-2ACEPROMAZINE MALEATE500 in 1 BOTTLETABLET5001
11695-7034-1ACEPROMAZINE MALEATE100 in 1 BOTTLETABLET1001
11695-7034-2ACEPROMAZINE MALEATE500 in 1 BOTTLETABLET5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11695-7033ACEPROMAZINE MALEATE TABLET [COVETRUS NORTH AMERICA]12 package rows20241116_934fcdff-5ae4-48f5-baa0-ddf549662a56.zip
11695-7034ACEPROMAZINE MALEATE TABLET [COVETRUS NORTH AMERICA]12 package rows20241116_934fcdff-5ae4-48f5-baa0-ddf549662a56.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11695-703411695-7034-1, 11695-7034-2
11695-703311695-7033-1, 11695-7033-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACEPROMAZINE MALEATE37862HP2OMACTIB
ACEPROMAZINE MALEATE37862HP2OMACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.