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Bupropion Hydrochloride

NDC 72241-021 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerModavar Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208606
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (100 mg/1)
Marketing started20200116
Package count3

External sources

Source: openFDA. Public-domain (CC0).