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
47335-639-83	47335-639	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE (47335-639-83)
47335-639-81	47335-639	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET in 1 BOTTLE (47335-639-81)
47335-684-83	47335-684	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET in 1 BOTTLE (47335-684-83)
47335-685-13	47335-685	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET in 1 BOTTLE (47335-685-13)
47335-685-81	47335-685	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET in 1 BOTTLE (47335-685-81)
47335-685-83	47335-685	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET in 1 BOTTLE (47335-685-83)
47335-639-13	47335-639	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET in 1 BOTTLE (47335-639-13)
47335-684-13	47335-684	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET in 1 BOTTLE (47335-684-13)
47335-684-81	47335-684	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET in 1 BOTTLE (47335-684-81)
70518-3961-0	70518-3961	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20231214	N/A	ANDA	ANDA208066	REMEDYREPACK INC.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BLISTER PACK (70518-3961-0)
47335-578-81	47335-578	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE (47335-578-81)
47335-579-81	47335-579	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET in 1 BOTTLE (47335-579-81)
47335-579-83	47335-579	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET in 1 BOTTLE (47335-579-83)
47335-578-83	47335-578	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (47335-578-83)
47335-579-13	47335-579	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET in 1 BOTTLE (47335-579-13)
47335-578-13	47335-578	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET	ORAL	20230220	N/A	ANDA	ANDA208066	Sun Pharmaceutical Industries, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET in 1 BOTTLE (47335-578-13)