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
67877-641-90	67877-641	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-641-90)
0904-7359-04	0904-7359	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA212244	Major Pharmaceuticals	LURASIDONE HYDROCHLORIDE	120 mg/1	30 BLISTER PACK in 1 CARTON (0904-7359-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60687-769-94	60687-769	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230509	N/A	ANDA	ANDA212244	American Health Packaging	LURASIDONE HYDROCHLORIDE	60 mg/1	20 BLISTER PACK in 1 CARTON (60687-769-94) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-769-11)
67877-638-05	67877-638	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-638-05)
67877-638-30	67877-638	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-638-30)
67877-638-38	67877-638	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (67877-638-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-638-33)
67877-638-90	67877-638	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-638-90)
67877-642-05	67877-642	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-642-05)
67877-642-30	67877-642	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-642-30)
67877-642-38	67877-642	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	10 BLISTER PACK in 1 CARTON (67877-642-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-642-33)
67877-642-90	67877-642	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230104	N/A	ANDA	ANDA212244	Ascend Laboratories, LLC	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67877-642-90)