NDC11 59651056360
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 |
|---|---|
| 59651-0563-60 | 59651-0563 |
| 59651-563-60 | 59651-563 |
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 |
|---|---|---|---|---|---|---|
| RUFINAMIDE | RUFINAMIDE | Aurobindo Pharma Limited | 444544f0-7622-4eef-b218-f241bd50d4af | 2025-12-11 | Warnings, Adverse reactions | 59651-563-60 59651-563 59651056360 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.