NDC11 51817058601
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 |
|---|---|
| 51817-0586-01 | 51817-0586 |
| 51817-0586-1 | 51817-0586 |
| 51817-586-01 | 51817-586 |
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 |
|---|---|---|---|---|---|---|
| Bortezomib | BORTEZOMIB | Pharmascience Inc. | 191d231a-1fbd-4a65-9d33-d5dc03bac381 | 2022-05-02 | Warnings, Adverse reactions | 51817-586-01 51817-586 51817058601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.