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BUPROPION HYDROCHLORIDE (SR)

NDC 69097-879 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerCipla USA Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA206674
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20160725
Package count4

External sources

Source: openFDA. Public-domain (CC0).