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bupropion Hydrochloride

NDC 23155-192 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206975
Dosage form / routeTABLET · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (100 mg/1)
Marketing started20160819
Package count2

External sources

Source: openFDA. Public-domain (CC0).