NDC11 65219058401
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 |
|---|---|
| 65219-0584-01 | 65219-0584 |
| 65219-0584-1 | 65219-0584 |
| 65219-584-01 | 65219-584 |
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 |
|---|---|---|---|---|---|---|
| TYENNE | TOCILIZUMAB-AAZG | Fresenius Kabi USA, LLC | ad76441d-da59-47df-8d9d-2243005180f0 | 2026-08-26 | Boxed warning, Warnings, Adverse reactions | 65219-584-01 65219-584 65219058401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.