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"81968-345-01" National Drug Code (NDC)

Auvelity 1 KIT in 1 KIT (81968-345-01) * 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 BOTTLE * 30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE
(Axsome Therapeutics, Inc.)

NDC Code81968-345-01
Package Description1 KIT in 1 KIT (81968-345-01) * 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 BOTTLE * 30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE
Product NDC81968-345
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAuvelity
Non-Proprietary NameDextromethorphan Hydrobromide, Bupropion Hydrochloride
Dosage FormKIT
Start Marketing Date20260601
Marketing Category NameNDA
Application NumberNDA215430
ManufacturerAxsome Therapeutics, Inc.

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