NDC11 27241011805
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 |
|---|---|
| 27241-0118-05 | 27241-0118 |
| 27241-0118-5 | 27241-0118 |
| 27241-118-05 | 27241-118 |
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 | Ajanta Pharma USA Inc. | da2f0ba4-7c16-4fb0-bc1c-45540e8fefbf | 2025-10-01 | Warnings, Adverse reactions | 27241-118-05 27241-118 27241011805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.