FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE

NDC 59651-874 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075491
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (75 mg/1)
Marketing started20240425
Package count1

External sources

Source: openFDA. Public-domain (CC0).