NDC 71052-140-01 - 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
- Requested NDC
- 71052-140-01
- 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 | Type |
|---|---|---|---|
| Idoxuridine - DARMERICA, LLC | DARMERICA, LLC | 2026-01-09 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | 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#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.