FDA.reportPublic FDA data

NDC 73309-039-01 - Vidarabine

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
73309-039
Requested NDC
73309-039-01
Package NDCs from labels
73309-039-01
Manufacturer
Bluebay Shandong Co, LTD. | Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
Effective date
2019-10-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VidarabineBluebay Shandong Co, LTD. | Nanjing Chemlin Biomedical Science & Technology Co, Ltd.2019-10-16BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-039-01Vidarabine50 g in 1 JARPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-039VIDARABINE POWDER [BLUEBAY SHANDONG CO, LTD.]11 package rows20191017_f2842526-9fe8-4784-8e75-5b2f53a64d7a.zip

Reported adverse events (FAERS/openFDA)#

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