FDA NDC Directory · JSON-LD · Markdown

Bupropion hydrochloride

NDC 47335-736 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078866
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (100 mg/1)
Marketing started20200301
Package count4

External sources

Source: openFDA. Public-domain (CC0).