NDC11 50474078078
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 |
|---|---|
| 50474-0780-78 | 50474-0780 |
| 50474-780-78 | 50474-780 |
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 |
|---|---|---|---|---|---|---|
| Bimzelx | BIMEKIZUMAB | UCB, Inc. | 26b88358-871f-4c80-9d80-b2fb16477f81 | 2025-06-16 | Warnings, Adverse reactions | 50474-780-78 50474-780 50474078078 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.