NDC11 50242009130
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 |
|---|---|
| 50242-0091-30 | 50242-0091 |
| 50242-091-30 | 50242-091 |
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 |
|---|---|---|---|---|---|---|
| Rozlytrek | ENTRECTINIB | Genentech, Inc. | c7c71b0c-2549-4495-86b6-c2807fa54908 | 2025-12-04 | Warnings, Adverse reactions | 50242-091-30 50242-091 50242009130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.