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Naproxen sodium

NDC 0480-0952 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namenaproxen sodium
Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075416
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNAPROXEN SODIUM (500 mg/1)
Marketing started20221101
Package count1

External sources

Source: openFDA. Public-domain (CC0).