NDC11 70518222705
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 |
|---|---|
| 70518-2227-05 | 70518-2227 |
| 70518-2227-5 | 70518-2227 |
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 | REMEDYREPACK INC. | 363cd347-d25e-42b9-9ce7-30642f3cb353 | 2026-06-25 | Warnings, Adverse reactions | 70518-2227-5 70518-2227 70518222705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.