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
53746-880-30	53746-880	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20240705	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals of New York LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (53746-880-30)
65162-879-03	65162-879	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE (65162-879-03)
65162-879-09	65162-879	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (65162-879-09)
65162-879-50	65162-879	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, COATED in 1 BOTTLE (65162-879-50)
53746-881-30	53746-881	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20240705	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals of New York LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, COATED in 1 BOTTLE (53746-881-30)
65162-880-03	65162-880	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (65162-880-03)
65162-880-09	65162-880	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (65162-880-09)
65162-880-50	65162-880	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, COATED in 1 BOTTLE (65162-880-50)
70518-3985-0	70518-3985	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20240119	N/A	ANDA	ANDA208002	REMEDYREPACK INC.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-3985-0)
53746-882-30	53746-882	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20240705	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals of New York LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, COATED in 1 BOTTLE (53746-882-30)
65162-881-03	65162-881	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, COATED in 1 BOTTLE (65162-881-03)
65162-881-09	65162-881	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, COATED in 1 BOTTLE (65162-881-09)
65162-881-50	65162-881	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, COATED in 1 BOTTLE (65162-881-50)
65162-082-03	65162-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BOTTLE (65162-082-03)
65162-082-09	65162-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, COATED in 1 BOTTLE (65162-082-09)
65162-082-50	65162-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET, COATED in 1 BOTTLE (65162-082-50)
53746-879-30	53746-879	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20240705	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals of New York LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE (53746-879-30)
65162-882-03	65162-882	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, COATED in 1 BOTTLE (65162-882-03)
65162-882-09	65162-882	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, COATED in 1 BOTTLE (65162-882-09)
65162-882-50	65162-882	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, COATED	ORAL	20230102	N/A	ANDA	ANDA208002	Amneal Pharmaceuticals LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, COATED in 1 BOTTLE (65162-882-50)