NDC11 71288041351
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 |
|---|---|
| 71288-0413-51 | 71288-0413 |
| 71288-413-51 | 71288-413 |
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 |
|---|---|---|---|---|---|---|
| Eptifibatide | EPTIFIBATIDE | Meitheal Pharmaceuticals Inc. | 3e7e7cd3-8efa-4d91-a5ab-7fd78b0cc65e | 2024-05-14 | Warnings, Adverse reactions | 71288-413-51 71288-413 71288041351 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.