FDA.reportPublic FDA data

NDC 73309-195-01 - 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
73309-195
Requested NDC
73309-195-01
Package NDCs from labels
73309-195-01, 73309-195-02, 73309-195-03, 73309-195-04
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2022-06-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mebendazole - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2022-06-17BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-195-01Mebendazole1 kg in 1 JARPOWDER15
73309-195-02Mebendazole5 kg in 1 DRUMPOWDER55
73309-195-03Mebendazole4.9 kg in 1 DRUMPOWDER4.95
73309-195-04Mebendazole0.5 kg in 1 JARPOWDER0.55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-195MEBENDAZOLE POWDER [BLUEBAY SHANDONG CO.,LTD]54 package rows20220623_660ecfdd-677d-4fe9-baa9-1308b6539bf9.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.