NDC11 72789031030
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 |
|---|---|
| 72789-0310-30 | 72789-0310 |
| 72789-310-30 | 72789-310 |
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 | PD-Rx Pharmaceuticals, Inc. | 2f5cee5c-ec55-4e9b-9d54-e7f2f052130e | 2026-02-26 | Warnings, Adverse reactions | 72789-310-30 72789-310 72789031030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.