FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE

NDC 72189-124 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA210497
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20200814
Package count2

External sources

Source: openFDA. Public-domain (CC0).