NDC11 80425053102
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 |
|---|---|
| 80425-0531-02 | 80425-0531 |
| 80425-0531-2 | 80425-0531 |
| 80425-531-02 | 80425-531 |
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 |
|---|---|---|---|---|---|---|
| Naproxen Sodium | NAPROXEN SODIUM | Advanced Rx of Tennessee, LLC | 369911ea-9069-9c45-e063-6394a90a5ce6 | 2026-02-12 | Boxed warning, Warnings, Adverse reactions | 80425-0531-2 80425-0531 80425053102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.