NDC11 00008451001
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 |
|---|---|
| 00008-4510-01 | 00008-4510 |
| 00008-4510-1 | 00008-4510 |
| 0008-4510-01 | 0008-4510 |
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 |
|---|---|---|---|---|---|---|
| Mylotarg | GEMTUZUMAB OZOGAMICIN | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 32fd2bb2-1cfa-4250-feb8-d7956c794e05 | 2025-12-19 | Boxed warning, Warnings, Adverse reactions | 0008-4510-01 0008-4510 00008451001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.