FDA.reportPublic FDA data

NDC 73309-119-03 - Idoxuridine

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
73309-119
Requested NDC
73309-119-03
Package NDCs from labels
73309-119-01, 73309-119-02, 73309-119-03
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-04-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Idoxuridine - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-04-14BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-119-01Idoxuridine100 g in 1 JARPOWDER1001
73309-119-02Idoxuridine10 g in 1 JARPOWDER101
73309-119-03Idoxuridine1 g in 1 JARPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-119IDOXURIDINE POWDER [BLUEBAY SHANDONG CO.,LTD]13 package rows20200415_03fab77c-991d-4f7d-9249-14de1c934ae2.zip

Reported adverse events (FAERS/openFDA)#

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