NDC11 84612085501
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 |
|---|---|
| 84612-0855-01 | 84612-0855 |
| 84612-0855-1 | 84612-0855 |
| 84612-855-01 | 84612-855 |
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 |
|---|---|---|---|---|---|---|
| WEZLANA | USTEKINUMAB-AUUB | Nuvaila Limited | a6c23978-09f0-4796-88f7-d0ce7e3ed04e | 2026-06-03 | Warnings, Adverse reactions | 84612-855-01 84612-855 84612085501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.