NDC 81968-345 – Auvelity

· Kit

Human Prescription Drug

Product NDC81968-345

Product details

Brand name
Auvelity
Generic name
Dextromethorphan hydrobromide, bupropion hydrochloride
Labeler
Axsome Therapeutics, Inc.
Dosage form
Kit
Marketing category
NDA · NDA215430
Marketed since
June 1, 2026
Listing expires
December 31, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Auvelity →

    Package NDC codes (2)

    Package NDCDescriptionSince
    81968-345-011 KIT in 1 KIT (81968-345-01) * 30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 21 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLEJun 1, 2026
    81968-345-03 sample1 KIT in 1 KIT (81968-345-03) * 30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 21 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLEJun 1, 2026

    Other Auvelity products