FDA.reportPublic FDA data

NDC 73309-123-01 - Sulfathiazole

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
73309-123
Requested NDC
73309-123-01
Package NDCs from labels
73309-123-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-04-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sulfathiazole - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-04-16BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-123-01Sulfathiazole500 g in 1 JARPOWDER5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-123SULFATHIAZOLE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20200417_3cd95f05-0738-49b7-834f-be7ab7b2079f.zip

Reported adverse events (FAERS/openFDA)#

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