FDA NDC Directory · JSON-LD · Markdown
NDC 71205-595 · HUMAN OTC DRUG · TABLET
| Generic name | Naproxen Sodium |
|---|---|
| Labeler / Manufacturer | Proficient Rx LP |
| Marketing category | Abbreviated NDA (generic) · App ANDA204872 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20190101 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).