FDA.reportPublic FDA data

NDC 10695-181-10 - Acepromazine Maleate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
10695-181
Requested NDC
10695-181-10
Package NDCs from labels
10695-181-10
Manufacturer
Willow Birch Pharma, Inc. | Sigma-Aldrich Ireland Ltd.
Effective date
2023-05-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Acepromazine Maleate - Willow Birch Pharma, Inc. | Sigma-Aldrich Ireland Ltd.Willow Birch Pharma, Inc. | Sigma-Aldrich Ireland Ltd.2023-05-16BULK INGREDIENT - ANIMAL DRUG

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

Reported adverse events (FAERS/openFDA)#

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