NDC 10695-138-10 - 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
Requested NDC: 10695-138-10
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
Label	Manufacturer	Effective date	Type
Ponazuril - Willow Birch Pharma, Inc. \| Alivira Animal Health Limited	Willow Birch Pharma, Inc. \| Alivira Animal Health Limited	2022-09-20	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10695-138-10	Ponazuril	1 kg in 1 PACKAGE	POWDER	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10695-138	PONAZURIL POWDER [WILLOW BIRCH PHARMA, INC.]	1	1 package rows	20220921_9f3700af-ab88-4fbf-8b77-0f1484aecd38.zip

Reported adverse events (FAERS/openFDA)#

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