NDC 86202-3108-1 - PHENBENDAZOLE

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: 86202-3108
Requested NDC: 86202-3108-1
Package NDCs from labels: 86202-3108-1
Manufacturer: AMBIENCE FAMILY INC
Effective date: 2024-06-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PHENBENDAZOLE - AMBIENCE FAMILY INC	AMBIENCE FAMILY INC	2024-06-19	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86202-3108-1	PHENBENDAZOLE	1.85 g in 1 CAPSULE	TABLET	1.85		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86202-3108	PHENBENDAZOLE TABLET [AMBIENCE FAMILY INC]	1	1 package rows	20240620_047e2bef-53c4-4c36-b13b-3d2ebd232f3e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PREPAKU FENBENDAZOLE Canine Dewormer	FENBENDAZOLE	Shenzhen Zhenshangzekai Technology Co., Ltd.	4d722051-6a49-75ea-e063-6294a90a7b4e	2026-03-20	Warnings	Exact identifier unii: 621BVT9M36
Fenbendazole 222 MG	FENBENDAZOLE 222 MG	B & L Healthcare Products INC	337c4554-2049-a725-e063-6394a90a66f5	2025-04-23	Warnings	Exact identifier unii: 621BVT9M36

Reported adverse events (FAERS/openFDA)#

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