NDC11 82804026972
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 |
|---|---|
| 82804-0269-72 | 82804-0269 |
| 82804-269-72 | 82804-269 |
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 | Proficient Rx LP | f4353734-29b0-4027-824d-2fc97f778c67 | 2026-02-01 | Warnings, Adverse reactions | 82804-269-72 82804-269 82804026972 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.