NDC11 59651093160
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 |
|---|---|
| 59651-0931-60 | 59651-0931 |
| 59651-931-60 | 59651-931 |
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 |
|---|---|---|---|---|---|---|
| everolimus | EVEROLIMUS | Aurobindo Pharma Limited | 43ef3c29-0e25-4fdd-aea1-06a20af9bbab | 2026-02-26 | Boxed warning, Warnings, Adverse reactions | 59651-931-60 59651-931 59651093160 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.