NDC11 51144000212
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 |
|---|---|
| 51144-0002-12 | 51144-0002 |
| 51144-002-12 | 51144-002 |
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 |
|---|---|---|---|---|---|---|
| TUKYSA | TUCATINIB | SEAGEN INC. | f27eb1b9-b7fc-424e-988f-84dd7bb195a3 | 2024-11-04 | Warnings, Adverse reactions | 51144-002-12 51144-002 51144000212 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.