FDA.reportPublic FDA data

NDC 10695-138 - Ponazuril

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
10695-138
Package NDCs from labels
10695-138-10
Manufacturer
Willow Birch Pharma, Inc. | Alivira Animal Health Limited
Effective date
2022-09-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ponazuril - Willow Birch Pharma, Inc. | Alivira Animal Health LimitedWillow Birch Pharma, Inc. | Alivira Animal Health Limited2022-09-20BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10695-138-10Ponazuril1 kg in 1 PACKAGEPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10695-138PONAZURIL POWDER [WILLOW BIRCH PHARMA, INC.]11 package rows20220921_9f3700af-ab88-4fbf-8b77-0f1484aecd38.zip