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BUPROPION HYDROCHLORIDE

NDC 42571-241 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameBupropion Hydrochloride
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207403
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (75 mg/1)
Marketing started20200701
Package count1

External sources

Source: openFDA. Public-domain (CC0).