FDA.reportPublic FDA data

Acepromazine Maleate

Manufacturer
Willow Birch Pharma, Inc. | Sigma-Aldrich Ireland Ltd.
Effective date
2023-05-16
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:50:44

Label at a glance#

ProductAcepromazine Maleate
Active ingredientACEPROMAZINE MALEATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10695-181-10Acepromazine Maleate1 kg in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10695-181ACEPROMAZINE MALEATE POWDER [WILLOW BIRCH PHARMA, INC.]11 package rows20230517_13f69ecc-5c71-497e-af4a-9dc96351d5b7.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
10695-18110695-181-10
54154-019

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ACEPROMAZINE MALEATE37862HP2OMACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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