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bupropion hydrochloride SR

NDC 0904-7465 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA202304
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20241115
Package count1

External sources

Source: openFDA. Public-domain (CC0).