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
68180-670-06	68180-670	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208031	Lupin Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (68180-670-06)
68180-671-06	68180-671	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208031	Lupin Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET in 1 BOTTLE (68180-671-06)
68180-672-06	68180-672	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208031	Lupin Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE (68180-672-06)
68180-673-06	68180-673	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208031	Lupin Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET in 1 BOTTLE (68180-673-06)
68180-674-06	68180-674	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208031	Lupin Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET in 1 BOTTLE (68180-674-06)