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Bupropion Hydrochloride SR

NDC 71335-1870 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA211347
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20201102
Package count6

External sources

Source: openFDA. Public-domain (CC0).