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
16729-348-10	16729-348	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208049	Accord Healthcare, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-348-10)
16729-349-10	16729-349	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208049	Accord Healthcare, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-349-10)
16729-346-10	16729-346	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208049	Accord Healthcare, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-346-10)
16729-350-10	16729-350	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208049	Accord Healthcare, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-350-10)
16729-347-10	16729-347	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208049	Accord Healthcare, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-347-10)
50090-6438-0	50090-6438	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230417	N/A	ANDA	ANDA208049	A-S Medication Solutions	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6438-0)