NDC11 55758004850
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 |
|---|---|
| 55758-0048-50 | 55758-0048 |
| 55758-048-50 | 55758-048 |
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 |
|---|---|---|---|---|---|---|
| Rapidol Naproxen | NAPROXEN SODIUM | Pharmadel LLC | c94c4b6e-a48b-cee5-e053-2995a90a49ac | 2026-03-20 | Warnings | 55758-048-50 55758-048 55758004850 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.