NDC11 59651080120
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 |
|---|---|
| 59651-0801-20 | 59651-0801 |
| 59651-801-20 | 59651-801 |
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 |
|---|---|---|---|---|---|---|
| ROFLUMILAST | ROFLUMILAST | Aurobindo Pharma Limited | 7cb11d48-6bb9-437b-bc7f-382050a2d3e6 | 2025-05-27 | Warnings, Adverse reactions | 59651-801-20 59651-801 59651080120 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.