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Bupropion Hydrochloride (XL)

NDC 43598-655 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerDr Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA207479
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20170412
Package count3

External sources

Source: openFDA. Public-domain (CC0).