NDC 71052-140 - 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: 71052-140
Package NDCs from labels: 71052-140-10, 71052-140-25, 71052-140-02, 71052-140-01
Manufacturer: DARMERICA, LLC
Effective date: 2026-01-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Idoxuridine - DARMERICA, LLC	DARMERICA, LLC	2026-01-09	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71052-140-01	Idoxuridine	0.001 kg in 1 PACKAGE	POWDER	0.001	5
71052-140-02	Idoxuridine	0.005 kg in 1 PACKAGE	POWDER	0.005	5
71052-140-10	Idoxuridine	0.1 kg in 1 PACKAGE	POWDER	0.1	5
71052-140-25	Idoxuridine	0.025 kg in 1 PACKAGE	POWDER	0.025	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71052-140	IDOXURIDINE POWDER [DARMERICA, LLC]	4	4 package rows	20241001_da91f89d-6e64-4097-97e4-c05c55fb7175.zip

Reported adverse events (FAERS/openFDA)#

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