FDA NDC Directory · JSON-LD · Markdown
NDC 47682-237 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | NAPROXEN SODIUM |
|---|---|
| Labeler / Manufacturer | Unifirst First Aid Corporation |
| Marketing category | Abbreviated NDA (generic) · App ANDA079096 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20081230 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).