FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE

NDC 59651-848 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090325
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20250603
Package count2

External sources

Source: openFDA. Public-domain (CC0).