FDA NDC Directory · JSON-LD · Markdown

WELLBUTRIN SR

NDC 0173-0722 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namebupropion hydrochloride
Labeler / ManufacturerGlaxoSmithKline LLC
Marketing categoryNew Drug Application (innovator) · App NDA020358
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (200 mg/1)
Marketing started20020625
Package count1

External sources

Source: openFDA. Public-domain (CC0).