NDC11 70710120801
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 |
|---|---|
| 70710-1208-01 | 70710-1208 |
| 70710-1208-1 | 70710-1208 |
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 |
|---|---|---|---|---|---|---|
| PLERIXAFOR | PLERIXAFOR | Zydus Pharmaceuticals USA Inc. | a0a058f9-1618-4853-9b8a-e9768ee86b39 | 2024-12-06 | Warnings, Adverse reactions | 70710-1208-1 70710-1208 70710120801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.