FDA NDC Directory · JSON-LD · Markdown
NDC 85509-1436 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | PHOENIX RX LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA212517 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | NAPROXEN (500 mg/1) |
| Marketing started | 20200301 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).