NDC11 80425053203
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 |
|---|---|
| 80425-0532-03 | 80425-0532 |
| 80425-0532-3 | 80425-0532 |
| 80425-532-03 | 80425-532 |
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 | 36996557-3227-b753-e063-6394a90a7b6f | 2026-02-12 | Boxed warning, Warnings, Adverse reactions | 80425-0532-3 80425-0532 80425053203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.