NDC 71052-169 - Mebendazole

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
71052-169
Package NDCs from labels
71052-169-01, 71052-169-02, 71052-169-50, 71052-169-10, 71052-169-15, 71052-169-05
Manufacturer
DARMERICA, LLC
Effective date
2026-04-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mebendazole - DARMERICA, LLCDARMERICA, LLC2026-04-20BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-169-01Mebendazole1 kg in 1 PACKAGEPOWDER18
71052-169-02Mebendazole20 kg in 1 PACKAGEPOWDER208
71052-169-05Mebendazole5 kg in 1 PACKAGEPOWDER58
71052-169-10Mebendazole0.1 kg in 1 PACKAGEPOWDER0.18
71052-169-15Mebendazole15 kg in 1 PACKAGEPOWDER158
71052-169-50Mebendazole0.5 kg in 1 PACKAGEPOWDER0.58

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-169MEBENDAZOLE POWDER [DARMERICA, LLC]76 package rows20250424_b500b5b7-622e-47c1-a4bc-d22210caa15a.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
VERMOXMEBENDAZOLEJanssen Pharmaceuticals, Inc.a720c424-517a-461b-8e13-6c37caf8aa3f2021-10-05Warnings, Adverse reactionsExact identifier
unii: 81G6I5V05I

Reported adverse events (FAERS/openFDA)#

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