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Bupropion Hydrochloride XL

NDC 0904-7505 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameBupropion Hydrochloride
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090693
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20241125
Package count2

External sources

Source: openFDA. Public-domain (CC0).