NDC 10695-093-50 - 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: 10695-093
Requested NDC: 10695-093-50
Package NDCs from labels: 10695-093-50
Manufacturer: Willow Birch Pharma, Inc.
Effective date: 2021-09-01
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.	Willow Birch Pharma, Inc.	2021-09-01	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10695-093-50	Ponazuril	5 kg in 1 CONTAINER	POWDER	5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10695-093	PONAZURIL POWDER [WILLOW BIRCH PHARMA, INC.]	1	1 package rows	20210903_caf26d6a-7b61-2732-e053-2995a90ad809.zip

Reported adverse events (FAERS/openFDA)#

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