NDC11 65597080101
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 |
|---|---|
| 65597-0801-01 | 65597-0801 |
| 65597-0801-1 | 65597-0801 |
| 65597-801-01 | 65597-801 |
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 |
|---|---|---|---|---|---|---|
| DATROWAY | DATOPOTAMAB DERUXTECAN | Daiichi Sankyo Inc. | 2950227c-6230-4ca4-a135-46e44d9424a0 | 2026-05-27 | Warnings, Adverse reactions | 65597-801-01 65597-801 65597080101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.