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Bupropion Hydrochloride XL

NDC 76420-923 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077715
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20081126
Package count5

External sources

Source: openFDA. Public-domain (CC0).