NDC11 71288042792
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 |
|---|---|
| 71288-0427-92 | 71288-0427 |
| 71288-427-92 | 71288-427 |
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 |
|---|---|---|---|---|---|---|
| BIVALIRUDIN | BIVALIRUDIN | Meitheal Pharmaceuticals Inc. | 26fb46f6-0088-42b8-b6f2-c67224776803 | 2024-04-04 | Warnings, Adverse reactions | 71288-427-92 71288-427 71288042792 |
| BIVALIRUDIN | BIVALIRUDIN | Meitheal Pharmaceuticals Inc. | 4119b710-ef30-4e3e-b99a-38e42b4b3fca | 2021-06-08 | Warnings, Adverse reactions | 71288-427 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.