NDC11 42385093530
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 |
|---|---|
| 42385-0935-30 | 42385-0935 |
| 42385-935-30 | 42385-935 |
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 | Laurus Labs Limited | 8e58c13a-8088-4fed-86cc-52530de5aa45 | 2022-12-28 | Warnings, Adverse reactions | 42385-935-30 42385-935 42385093530 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.