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Naproxen

NDC 80425-0050 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078250
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN (500 mg/1)
Marketing started20070701
Package count2

External sources

Source: openFDA. Public-domain (CC0).