NDC11 59651021690
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 |
|---|---|
| 59651-0216-90 | 59651-0216 |
| 59651-216-90 | 59651-216 |
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 |
|---|---|---|---|---|---|---|
| FENOFIBRIC ACID | FENOFIBRIC ACID | Aurobindo Pharma Limited | 9ad201de-fa62-4c49-bc61-ee09b9ba434c | 2025-08-02 | Warnings, Adverse reactions | 59651-216-90 59651-216 59651021690 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.