NDC11 69097089602
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 |
|---|---|
| 69097-0896-02 | 69097-0896 |
| 69097-0896-2 | 69097-0896 |
| 69097-896-02 | 69097-896 |
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 |
|---|---|---|---|---|---|---|
| Fenofibrate | FENOFIBRATE | Cipla USA Inc., | 07d47c02-ab29-4ba9-aea0-96ffbd70c0ef | 2023-01-20 | Warnings, Adverse reactions | 69097-896-02 69097-896 69097089602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.