NDC11 62135089490
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 |
|---|---|
| 62135-0894-90 | 62135-0894 |
| 62135-894-90 | 62135-894 |
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 | Chartwell RX, LLC. | 2d0cfddc-ace3-4187-8d94-d760d23d20b6 | 2025-12-10 | Warnings, Adverse reactions | 62135-894-90 62135-894 62135089490 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.