FDA NDC

AUVELITY

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
81968-030
Proprietary name
AUVELITY
Nonproprietary name
dextromethorphan hydrobromide, bupropion hydrochloride
Labeler
Axsome Therapeutics, Inc.
Dosage form
TABLET, MULTILAYER, EXTENDED RELEASE
Strength
30 mg/1

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