NDC11 50419039303
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 |
|---|---|
| 50419-0393-03 | 50419-0393 |
| 50419-0393-3 | 50419-0393 |
| 50419-393-03 | 50419-393 |
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 |
|---|---|---|---|---|---|---|
| VITRAKVI | LAROTRECTINIB | Bayer HealthCare Pharmaceuticals Inc. | 0c8ca614-58b2-4aa4-83d3-0387a8f782fd | 2026-05-22 | Warnings, Adverse reactions | 50419-393-03 50419-393 50419039303 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.