FDA.reportPublic FDA data

NDC 73309-221-01 - Sulfadimethoxine

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
73309-221
Requested NDC
73309-221-01
Package NDCs from labels
73309-221-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-01-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sulfadimethoxine - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-01-28BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-221-01Sulfadimethoxine500 g in 1 JARPOWDER5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-221SULFADIMETHOXINE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20210129_b775a94e-1423-463a-9d1f-eb7be664ed07.zip

Reported adverse events (FAERS/openFDA)#

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