NDC11 69367025409
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 |
|---|---|
| 69367-0254-09 | 69367-0254 |
| 69367-0254-9 | 69367-0254 |
| 69367-254-09 | 69367-254 |
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 | Westminster Pharmaceuticals, LLC | a97ebf51-4f68-4426-9958-5c59f91b1d47 | 2026-05-22 | Warnings, Adverse reactions | 69367-254-09 69367-254 69367025409 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.