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Naproxen Sodium

NDC 62207-729 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules India Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA091353
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20180608
Package count5

External sources

Source: openFDA. Public-domain (CC0).