FDA.reportPublic FDA data

NDC 73309-199-01 - Metronidazole Benzoate

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
73309-199
Requested NDC
73309-199-01
Package NDCs from labels
73309-199-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-09-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Metronidazole Benzoate - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-09-30BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-199-01Metronidazole Benzoate500 g in 1 JARPOWDER5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-199METRONIDAZOLE BENZOATE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20201001_ac8ba49c-e5eb-4644-a560-5e9a60912e5f.zip

Reported adverse events (FAERS/openFDA)#

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