FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE

NDC 59651-511 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216051
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20260721
Package count3

External sources

Source: openFDA. Public-domain (CC0).