FDA NDC Directory · JSON-LD · Markdown
NDC 62207-761 · HUMAN OTC DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Granules India Ltd |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA091353 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20110930 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).