FDA NDC Directory · JSON-LD · Markdown
NDC 0280-6000 · HUMAN OTC DRUG · TABLET
| Generic name | NAPROXEN SODIUM |
|---|---|
| Labeler / Manufacturer | Bayer HealthCare LLC. |
| Marketing category | New Drug Application (innovator) · App NDA020204 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20140226 |
| Package count | 16 |
Source: openFDA. Public-domain (CC0).