NDC11 65862069278
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 |
|---|---|
| 65862-0692-78 | 65862-0692 |
| 65862-692-78 | 65862-692 |
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 |
|---|---|---|---|---|---|---|
| Extended Phenytoin Sodium | PHENYTOIN SODIUM | Aurobindo Pharma Limited | 5362ea50-38a4-48b4-a85b-d634c3d8b91a | 2023-09-21 | Warnings, Adverse reactions | 65862-692-78 65862-692 65862069278 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.