FDA.reportPublic FDA data

Vidarabine

Manufacturer
Bluebay Shandong Co, LTD. | Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
Effective date
2019-10-16
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:23

Label at a glance#

ProductVidarabine
Active ingredientVIDARABINE
Label structure1 sections

Label contents#

Full prescribing information#

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VidarabineVidarabine

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-03973309-039-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
VIDARABINEFA2DM6879KACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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