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
33342-419-07	33342-419	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-419-07)
33342-419-10	33342-419	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-419-10)
33342-420-07	33342-420	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-420-07)
33342-420-10	33342-420	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-420-10)
33342-421-07	33342-421	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-421-07)
33342-421-10	33342-421	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-421-10)
33342-422-07	33342-422	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-422-07)
33342-422-10	33342-422	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-422-10)
33342-423-07	33342-423	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-423-07)
33342-423-10	33342-423	HUMAN PRESCRIPTION DRUG	lurasidone hydrochloride	lurasidone hydrochloride	TABLET, FILM COATED	ORAL	20230609	N/A	ANDA	ANDA212124	Macleods Pharmaceuticals Limited	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-423-10)