NDC11 50268071913
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 |
|---|---|
| 50268-0719-13 | 50268-0719 |
| 50268-719-13 | 50268-719 |
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 |
|---|---|---|---|---|---|---|
| Phenytoin Sodium | PHENYTOIN SODIUM | AvPAK | 4c2542b8-ac54-e85d-e063-6294a90a759b | 2026-03-03 | Warnings, Adverse reactions | 50268-719-13 50268-719 50268071913 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.