FDA.reportPublic FDA data

Idoxuridine

Manufacturer
DARMERICA, LLC
Effective date
2026-01-09
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
5
Source
monthly-update
Hydrated at
2026-06-03 17:53:29

Label at a glance#

ProductIdoxuridine
Active ingredientIdoxuridine
Label structure1 sections

Label contents#

Full prescribing information#

Idoxuridine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IdoxuridineIdoxuridine

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-140-01Idoxuridine0.001 kg in 1 PACKAGEPOWDER0.0015
71052-140-02Idoxuridine0.005 kg in 1 PACKAGEPOWDER0.0055
71052-140-10Idoxuridine0.1 kg in 1 PACKAGEPOWDER0.15
71052-140-25Idoxuridine0.025 kg in 1 PACKAGEPOWDER0.0255

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
71052-14071052-140-10, 71052-140-25, 71052-140-02, 71052-140-01

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
IdoxuridineLGP81V5245ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-09-30full-release2026-06-01 02:51:09

Reported adverse events (FAERS/openFDA)#

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