NDC11 75626000102
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 |
|---|---|
| 75626-0001-02 | 75626-0001 |
| 75626-0001-2 | 75626-0001 |
| 75626-001-02 | 75626-001 |
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 |
|---|---|---|---|---|---|---|
| LUPKYNIS | VOCLOSPORIN | Aurinia Pharma U.S., Inc. | 9f489295-1156-52c7-5fd0-5c4c52f9b813 | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | 75626-001-02 75626-001 75626000102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.