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WELLBUTRIN XL

NDC 0187-0731 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namebupropion hydrochloride
Labeler / ManufacturerBausch Health US LLC
Marketing categoryNew Drug Application (innovator) · App NDA021515
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20030829
Package count2

External sources

Source: openFDA. Public-domain (CC0).