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BUPROPION HYDROCHLORIDE

NDC 70010-127 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218385
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20250331
Package count3

External sources

Source: openFDA. Public-domain (CC0).