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Bupropion Hydrochloride

NDC 70518-1566 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076143
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (75 mg/1)
Marketing started20181222
Package count1

External sources

Source: openFDA. Public-domain (CC0).