NDC11 50242091786
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 |
|---|---|
| 50242-0917-86 | 50242-0917 |
| 50242-917-86 | 50242-917 |
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 |
|---|---|---|---|---|---|---|
| TECENTRIQ | ATEZOLIZUMAB | Genentech, Inc. | 6fa682c9-a312-4932-9831-f286908660ee | 2026-05-20 | Warnings, Adverse reactions | 50242-917-86 50242-917 50242091786 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.