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Nabumetone

NDC 50228-466 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerScieGen Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (750 mg/1)
Marketing started20190626
Package count3

External sources

Source: openFDA. Public-domain (CC0).