NDC 81968-453 – Auvelity

· Kit

Human Prescription Drug

Product NDC81968-453

Product details

Brand name
Auvelity
Generic name
dextromethorphan hydrobromide, bupropion hydrochloride
Labeler
Axsome Therapeutics, Inc.
Dosage form
Kit
Marketing category
NDA · NDA215430
Marketed since
July 30, 2026
Listing expires
December 31, 2027

Active ingredients

    Uses, dosage, side effects and warnings for Auvelity →

    Package NDC codes (1)

    Package NDCDescriptionSince
    81968-453-01 sample1 KIT in 1 KIT (81968-453-01) * 1 BOTTLE in 1 CARTON / 21 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLEJul 30, 2026

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