NDC11 58151011088
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 |
|---|---|
| 58151-0110-88 | 58151-0110 |
| 58151-110-88 | 58151-110 |
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 |
|---|---|---|---|---|---|---|
| DILANTIN | EXTENDED PHENYTOIN SODIUM | Viatris Specialty LLC | 86dd27d1-9cee-48ae-b55d-e2d2f7dbc593 | 2023-08-21 | Warnings, Adverse reactions | 58151-110-88 58151-110 58151011088 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.