NDC11 50242009002
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 |
|---|---|
| 50242-0090-02 | 50242-0090 |
| 50242-0090-2 | 50242-0090 |
| 50242-090-02 | 50242-090 |
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 |
|---|---|---|---|---|---|---|
| ZELBORAF | VEMURAFENIB | Genentech, Inc. | 38eea320-7e0c-485a-bc30-98c3c45e2763 | 2026-08-28 | Warnings, Adverse reactions | 50242-090-02 50242-090 50242009002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.