FDA.reportPublic FDA data

Idoxuridine

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-04-14
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:34

Label at a glance#

ProductIdoxuridine
Active ingredientIDOXURIDINE
Label structure1 sections

Label contents#

Full prescribing information#

Idoxuridine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-11973309-119-01, 73309-119-02, 73309-119-03

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
IDOXURIDINELGP81V5245ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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