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
70518-4126-0	70518-4126	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20240701	N/A	ANDA	ANDA208052	REMEDYREPACK INC.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-4126-0)
70771-1734-4	70771-1734	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (70771-1734-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1734-2)
70771-1734-9	70771-1734	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (70771-1734-9)
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)
70771-1736-1	70771-1736	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (70771-1736-1)
70771-1736-3	70771-1736	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, COATED in 1 BOTTLE (70771-1736-3)
70771-1736-4	70771-1736	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	10 BLISTER PACK in 1 CARTON (70771-1736-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1736-2)
70771-1736-5	70771-1736	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET, COATED in 1 BOTTLE (70771-1736-5)
70771-1736-9	70771-1736	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, COATED in 1 BOTTLE (70771-1736-9)
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)
70771-1738-1	70771-1738	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	100 TABLET, COATED in 1 BOTTLE (70771-1738-1)
70771-1738-3	70771-1738	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, COATED	ORAL	20230201	N/A	ANDA	ANDA208052	Zydus Lifesciences Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, COATED in 1 BOTTLE (70771-1738-3)