NDC11 82804008531
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 |
|---|---|
| 82804-0085-31 | 82804-0085 |
| 82804-085-31 | 82804-085 |
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 |
|---|---|---|---|---|---|---|
| ELIQUIS | APIXABAN | Proficient Rx LP | 33752f5d-2ca7-45c0-8292-b54742219b97 | 2024-06-01 | Boxed warning, Warnings, Adverse reactions | 82804-085-31 82804-085 82804008531 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.