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AUVELITY

NDC 81968-030 · HUMAN PRESCRIPTION DRUG · TABLET, MULTILAYER, EXTENDED RELEASE

Generic namedextromethorphan hydrobromide, bupropion hydrochloride
Labeler / ManufacturerAxsome Therapeutics, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA215430
Dosage form / routeTABLET, MULTILAYER, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (105 mg/1)
DEXTROMETHORPHAN HYDROBROMIDE (30 mg/1)
Marketing started20260508
Package count1

External sources

Source: openFDA. Public-domain (CC0).