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bupropion hydrochloride SR

NDC 43547-290 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerSolco Healthcare US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202304
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20141101
Package count4

External sources

Source: openFDA. Public-domain (CC0).