NDC11 68180038809
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 |
|---|---|
| 68180-0388-09 | 68180-0388 |
| 68180-0388-9 | 68180-0388 |
| 68180-388-09 | 68180-388 |
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 | Lupin Pharmaceuticals, Inc. | 45364845-c3b4-40a1-a677-82202ffaa5ad | 2025-11-19 | Warnings, Adverse reactions | 68180-388-09 68180-388 68180038809 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.