NDC11 59922064260
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 |
|---|---|
| 59922-0642-60 | 59922-0642 |
| 59922-642-60 | 59922-642 |
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 |
|---|---|---|---|---|---|---|
| VAFSEO | VADADUSTAT | Akebia Therapeutics, Inc. | ac9da724-5a62-4ab6-a89c-376a25f6195b | 2026-03-30 | Boxed warning, Warnings, Adverse reactions | 59922-642-60 59922-642 59922064260 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.