NDC11 62332036071
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 |
|---|---|
| 62332-0360-71 | 62332-0360 |
| 62332-360-71 | 62332-360 |
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 | Alembic Pharmaceuticals Inc. | 5c579378-e00e-4802-b9d3-c062cf8bd9f4 | 2025-07-15 | Warnings, Adverse reactions | 62332-360-71 62332-360 62332036071 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.