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
70771-1735-1	70771-1735	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (70771-1735-1)
70771-1735-3	70771-1735	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230323	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (70771-1735-3)
70771-1735-4	70771-1735	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	10 BLISTER PACK in 1 CARTON (70771-1735-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1735-2)
70771-1735-5	70771-1735	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, COATED in 1 BOTTLE (70771-1735-5)
70771-1735-9	70771-1735	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (70771-1735-9)
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)
70771-1737-1	70771-1737	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	100 TABLET, COATED in 1 BOTTLE (70771-1737-1)
70771-1737-3	70771-1737	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, COATED in 1 BOTTLE (70771-1737-3)
70771-1737-4	70771-1737	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	10 BLISTER PACK in 1 CARTON (70771-1737-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1737-2)
70771-1737-5	70771-1737	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, COATED in 1 BOTTLE (70771-1737-5)
70771-1737-9	70771-1737	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, COATED in 1 BOTTLE (70771-1737-9)
68382-966-01	68382-966	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (68382-966-01)
68382-966-05	68382-966	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, COATED in 1 BOTTLE (68382-966-05)
68382-966-06	68382-966	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230323	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (68382-966-06)
68382-966-16	68382-966	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (68382-966-16)
68382-966-77	68382-966	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Pharmaceuticals USA Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	100 BLISTER PACK in 1 CARTON (68382-966-77) / 1 TABLET, COATED in 1 BLISTER PACK (68382-966-30)