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
13668-509-30	13668-509	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230217	N/A	ANDA	ANDA208047	Torrent Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-509-30)
70518-4132-0	70518-4132	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA208047	REMEDYREPACK INC.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4132-0)
70518-4117-0	70518-4117	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20240627	N/A	ANDA	ANDA208047	REMEDYREPACK INC.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0)
43598-351-05	43598-351	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (43598-351-05)
43598-352-05	43598-352	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (43598-352-05)
43598-352-30	43598-352	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-352-30)
43598-352-78	43598-352	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	40 mg/1	10 BLISTER PACK in 1 CARTON (43598-352-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-352-79)
43598-352-90	43598-352	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-352-90)
43598-353-05	43598-353	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (43598-353-05)
43598-353-30	43598-353	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-353-30)
43598-351-30	43598-351	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)
43598-351-78	43598-351	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (43598-351-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-351-79)
43598-351-90	43598-351	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-351-90)
43598-353-78	43598-353	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	60 mg/1	10 BLISTER PACK in 1 CARTON (43598-353-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-353-79)
43598-354-78	43598-354	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	80 mg/1	10 BLISTER PACK in 1 CARTON (43598-354-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-354-79)
43598-354-90	43598-354	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-354-90)
43598-353-90	43598-353	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-353-90)
43598-354-05	43598-354	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (43598-354-05)
43598-354-30	43598-354	HUMAN PRESCRIPTION DRUG	Lurasidone hydrochloride	Lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208047	Dr. Reddys Laboratories Inc	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-354-30)