NDC 84187-020-10 - Fenbendazole

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: 84187-020
Requested NDC: 84187-020-10
Package NDCs from labels: 84187-020-01, 84187-020-05, 84187-020-10, 84187-020-25
Manufacturer: AMGIS LIFESCIENCE LIMITED
Effective date: 2026-02-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Fenbendazole - AMGIS LIFESCIENCE LIMITED	AMGIS LIFESCIENCE LIMITED	2026-02-23	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
84187-020-01	Fenbendazole	1 kg in 1 DRUM	POWDER	1	2
84187-020-05	Fenbendazole	5 kg in 1 DRUM	POWDER	5	2
84187-020-10	Fenbendazole	10 kg in 1 DRUM	POWDER	10	2
84187-020-25	Fenbendazole	25 kg in 1 DRUM	POWDER	25	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84187-020	FENBENDAZOLE POWDER [AMGIS LIFESCIENCE LIMITED]	1	4 package rows	20241030_0bd800d2-e29b-4198-8994-c07a57560939.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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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.