NDC11 50242013086
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 |
|---|---|
| 50242-0130-86 | 50242-0130 |
| 50242-130-86 | 50242-130 |
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 |
|---|---|---|---|---|---|---|
| ALECENSA | ALECTINIB HYDROCHLORIDE | Genentech, Inc. | 42c49deb-713b-427a-9670-08af08adcffb | 2026-08-21 | Warnings, Adverse reactions | 50242-130-86 50242-130 50242013086 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.