NDC11 70709019212
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 |
|---|---|
| 70709-0192-12 | 70709-0192 |
| 70709-192-12 | 70709-192 |
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 |
|---|---|---|---|---|---|---|
| CAVHANZA | NILOTINIB | Cycle Pharmaceuticals Ltd | 98b197ea-bca4-427e-8737-97f70a3262bc | 2026-08-07 | Boxed warning, Warnings, Adverse reactions | 70709-192-12 70709-192 70709019212 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.