FDA NDC Directory · JSON-LD · Markdown

bupropion Hydrochloride

NDC 71610-866 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206975
Dosage form / routeTABLET · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (75 mg/1)
Marketing started20160819
Package count4

External sources

Source: openFDA. Public-domain (CC0).