FDA NDC Directory · JSON-LD · Markdown
NDC 0280-6090 · HUMAN OTC DRUG · TABLET
| Generic name | naproxen sodium, pseudeoephedrine hydrochloride |
|---|---|
| Labeler / Manufacturer | Bayer HealthCare LLC. |
| Marketing category | Abbreviated NDA (generic) · App ANDA076518 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1) |
| Marketing started | 20140101 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).