NDC11 71656001260
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 |
|---|---|
| 71656-0012-60 | 71656-0012 |
| 71656-012-60 | 71656-012 |
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 |
|---|---|---|---|---|---|---|
| CYCLOSPORINE | CYCLOSPORINE | Saptalis Pharmaceuticals, LLC | ff4dc2fc-667a-489a-b798-8d11cddfe716 | 2025-12-09 | Warnings, Adverse reactions | 71656-012-60 71656-012 71656001260 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.