NDC11 80513077103
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 80513-0771-03 | 80513-0771 |
| 80513-0771-3 | 80513-0771 |
| 80513-771-03 | 80513-771 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Antifungal | MICONAZOLE NITRATE | Advanced Rx LLC | e13eb653-3916-444a-ae86-1738c0308b79 | 2025-07-28 | Warnings | 80513-771-03 80513-771 80513077103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.