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Naproxen Sodium

NDC 55111-273 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075168
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started19980729
Package count6

External sources

Source: openFDA. Public-domain (CC0).