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Bupropion hydrochloride (XL)

NDC 69680-158 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion hydrochloride
Labeler / ManufacturerVitruvias Therapeutics
Marketing categoryAbbreviated NDA (generic) · App ANDA208652
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20230410
Package count4

External sources

Source: openFDA. Public-domain (CC0).