NDC11 00078063968
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 |
|---|---|
| 00078-0639-68 | 00078-0639 |
| 00078-639-68 | 00078-639 |
| 0078-0639-68 | 0078-0639 |
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 |
|---|---|---|---|---|---|---|
| COSENTYX | SECUKINUMAB | Novartis Pharmaceuticals Corporation | 77c4b13e-7df3-42d4-81db-3d0cddb7f67a | 2026-08-25 | Warnings, Adverse reactions | 0078-0639-68 0078-0639 00078063968 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.