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Bupropion Hydrochloride (SR)

NDC 33342-527 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218567
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20260623
Package count3

External sources

Source: openFDA. Public-domain (CC0).