FDA NDC Directory · JSON-LD · Markdown

Bupropion Hydrochloride

NDC 71610-899 · 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 started20250130
Package count3

External sources

Source: openFDA. Public-domain (CC0).