NDC11 70709011260
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 |
|---|---|
| 70709-0112-60 | 70709-0112 |
| 70709-112-60 | 70709-112 |
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 |
|---|---|---|---|---|---|---|
| HARLIKU | NITISINONE | Cycle Pharmaceuticals Ltd. | 7cf67e24-d46b-4376-bbd0-0b973c406d0d | 2025-06-02 | Warnings, Adverse reactions | 70709-112-60 70709-112 70709011260 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.