NDC11 59651046429
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 |
|---|---|
| 59651-0464-29 | 59651-0464 |
| 59651-464-29 | 59651-464 |
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 |
|---|---|---|---|---|---|---|
| SUNITINIB MALATE | SUNITINIB MALATE | Aurobindo Pharma Limited | 810dfcb2-d35b-4971-887c-2e78e82e9e07 | 2025-04-17 | Boxed warning, Warnings, Adverse reactions | 59651-464-29 59651-464 59651046429 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.