NDC11 71127200001
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 |
|---|---|
| 71127-2000-01 | 71127-2000 |
| 71127-2000-1 | 71127-2000 |
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 |
|---|---|---|---|---|---|---|
| Sevenfact | COAGULATION FACTOR VIIA RECOMBINANT HUMAN | Laboratoire Franais du Fractionnement et des Biotechnologies Socit Anonyme (LFB S.A.) | b23ad666-8ce0-4e0b-9eff-c6983ac5f7e6 | 2025-11-19 | Boxed warning, Warnings, Adverse reactions | 71127-2000-1 71127-2000 71127200001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.