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Bupropion Hydrochloride XL

NDC 50090-7112 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA210015
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20230430
Package count1

External sources

Source: openFDA. Public-domain (CC0).