NDC11 50458071000
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 |
|---|---|
| 50458-0710-0 | 50458-0710 |
| 50458-0710-00 | 50458-0710 |
| 50458-710-00 | 50458-710 |
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 |
|---|---|---|---|---|---|---|
| PONVORY | PONESIMOD | Janssen Pharmaceuticals, Inc | 5be69660-738c-4db7-b0d4-517aa873dc41 | 2025-04-25 | Warnings, Adverse reactions | 50458-710-00 50458071000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.