FDA NDC Directory · JSON-LD · Markdown
NDC 85237-1832 · HUMAN OTC DRUG · TABLET
| Generic name | NAPROXEN SODIUM |
|---|---|
| Labeler / Manufacturer | Select Consumer Group |
| Marketing category | New Drug Application (innovator) · App NDA020204 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20230404 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).