NDC11 00078067119
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 |
|---|---|
| 00078-0671-19 | 00078-0671 |
| 00078-671-19 | 00078-671 |
| 0078-0671-19 | 0078-0671 |
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 |
|---|---|---|---|---|---|---|
| TYKERB | LAPATINIB | Novartis Pharmaceuticals Corporation | eee37f88-ec6a-4c30-b8aa-e2c71f93088c | 2026-01-27 | Boxed warning, Warnings, Adverse reactions | 0078-0671-19 0078-0671 00078067119 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.