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
68382-967-06	68382-967	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, COATED in 1 BOTTLE (68382-967-06)
68382-967-16	68382-967	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, COATED in 1 BOTTLE (68382-967-16)
68382-967-77	68382-967	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	100 BLISTER PACK in 1 CARTON (68382-967-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-967-30)
68382-968-01	68382-968	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	100 TABLET, COATED in 1 BOTTLE (68382-968-01)
68382-968-05	68382-968	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, COATED in 1 BOTTLE (68382-968-05)
68382-968-06	68382-968	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, COATED in 1 BOTTLE (68382-968-06)
68382-968-16	68382-968	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, COATED in 1 BOTTLE (68382-968-16)
68382-968-77	68382-968	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	100 BLISTER PACK in 1 CARTON (68382-968-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-968-30)
68382-965-16	68382-965	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (68382-965-16)
68382-965-77	68382-965	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	100 BLISTER PACK in 1 CARTON (68382-965-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-965-30)
68382-965-01	68382-965	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	100 TABLET, COATED in 1 BOTTLE (68382-965-01)