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
31722-081-05	31722-081	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-081-05)
31722-081-30	31722-081	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-081-30)
31722-081-90	31722-081	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-081-90)
31722-082-05	31722-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-082-05)
31722-082-30	31722-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-082-30)
31722-082-90	31722-082	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	60 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-082-90)
31722-083-05	31722-083	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-083-05)
31722-083-30	31722-083	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-083-30)
31722-083-90	31722-083	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-083-90)
31722-084-05	31722-084	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-084-05)
31722-084-30	31722-084	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-084-30)
31722-084-90	31722-084	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	120 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-084-90)
31722-080-90	31722-080	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-080-90)
31722-080-30	31722-080	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-080-30)
31722-080-05	31722-080	HUMAN PRESCRIPTION DRUG	Lurasidone Hydrochloride	Lurasidone Hydrochloride	TABLET, FILM COATED	ORAL	20240821	N/A	ANDA	ANDA218174	Camber Pharmaceuticals, Inc.	LURASIDONE HYDROCHLORIDE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-080-05)