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
81968-351-01	81968-351	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-351-01)
81968-351-07	81968-351	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	150 mg/1	7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)
81968-351-10	81968-351	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	150 mg/1	10 BLISTER PACK in 1 CARTON (81968-351-10) / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)
81968-350-01	81968-350	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-350-01)
81968-350-07	81968-350	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	75 mg/1	7 TABLET, FILM COATED in 1 BLISTER PACK (81968-350-07)
81968-350-10	81968-350	HUMAN PRESCRIPTION DRUG	SUNOSI	solriamfetol	TABLET, FILM COATED	ORAL	20220602	N/A	NDA	NDA211230	Axsome Therapeutics, Inc.	SOLRIAMFETOL	75 mg/1	10 BLISTER PACK in 1 CARTON (81968-350-10) / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-350-07)