NDC11 59651079805
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 |
|---|---|
| 59651-0798-05 | 59651-0798 |
| 59651-0798-5 | 59651-0798 |
| 59651-798-05 | 59651-798 |
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 |
|---|---|---|---|---|---|---|
| FUROSEMIDE | FUROSEMIDE | Aurobindo Pharma Limited | a504ee4b-3995-45f2-898c-91116dd81d19 | 2025-07-19 | Warnings, Adverse reactions | 59651-798-05 59651-798 59651079805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.