FDA.reportPublic FDA data

NDC 84187-020 - 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
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
LabelManufacturerEffective dateType
Fenbendazole - AMGIS LIFESCIENCE LIMITEDAMGIS LIFESCIENCE LIMITED2026-02-23BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84187-020-01Fenbendazole1 kg in 1 DRUMPOWDER12
84187-020-05Fenbendazole5 kg in 1 DRUMPOWDER52
84187-020-10Fenbendazole10 kg in 1 DRUMPOWDER102
84187-020-25Fenbendazole25 kg in 1 DRUMPOWDER252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84187-020FENBENDAZOLE POWDER [AMGIS LIFESCIENCE LIMITED]14 package rows20241030_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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Fenbendazole 222 MGFENBENDAZOLE 222 MGB & L Healthcare Products INC337c4554-2049-a725-e063-6394a90a66f52025-04-23WarningsExact identifier
unii: 621BVT9M36

Reported adverse events (FAERS/openFDA)#

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