美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
81968-045-60	81968-045	HUMAN PRESCRIPTION DRUG	AUVELITY	dextromethorphan hydrobromide, bupropion hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20240628	N/A	NDA	NDA215430	Axsome Therapeutics, Inc.	BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE	105 mg/1; 45 mg/1	60 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (81968-045-60)
81968-045-31	81968-045	HUMAN PRESCRIPTION DRUG	AUVELITY	dextromethorphan hydrobromide, bupropion hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20240510	N/A	NDA	NDA215430	Axsome Therapeutics, Inc.	BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE	105 mg/1; 45 mg/1	1 BOTTLE in 1 CARTON (81968-045-31) / 30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE
81968-045-30	81968-045	HUMAN PRESCRIPTION DRUG	AUVELITY	dextromethorphan hydrobromide, bupropion hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20220818	N/A	NDA	NDA215430	Axsome Therapeutics, Inc.	BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE	105 mg/1; 45 mg/1	30 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (81968-045-30)
81968-045-14	81968-045	HUMAN PRESCRIPTION DRUG	AUVELITY	dextromethorphan hydrobromide, bupropion hydrochloride	TABLET, MULTILAYER, EXTENDED RELEASE	ORAL	20240918	N/A	NDA	NDA215430	Axsome Therapeutics, Inc.	BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE	105 mg/1; 45 mg/1	1 BOTTLE in 1 CARTON (81968-045-14) / 14 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE