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
69097-941-02	69097-941	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Cipla USA, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-941-02)
69097-942-02	69097-942	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Cipla USA, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-942-02)
69097-939-02	69097-939	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Cipla USA, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-939-02)
69097-938-02	69097-938	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Cipla USA, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-938-02)
69097-937-02	69097-937	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Cipla USA, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-937-02)
76282-522-30	76282-522	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Exelan Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-522-30)
76282-534-30	76282-534	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Exelan Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-534-30)
76282-523-30	76282-523	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Exelan Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-523-30)
76282-524-30	76282-524	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Exelan Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-524-30)
76282-525-30	76282-525	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20230220	N/A	ANDA	ANDA208028	Exelan Pharmaceuticals Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-525-30)