NDC11 51144000160
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 |
|---|---|
| 51144-0001-60 | 51144-0001 |
| 51144-001-60 | 51144-001 |
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 | 51144-001-60 51144-001 51144000160 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.