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
31722-434-30	31722-434	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	.25 mg/1	1 BOTTLE in 1 CARTON (31722-434-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-435-30	31722-435	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	.5 mg/1	1 BOTTLE in 1 CARTON (31722-435-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-436-30	31722-436	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	1 mg/1	1 BOTTLE in 1 CARTON (31722-436-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-437-30	31722-437	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	2 mg/1	1 BOTTLE in 1 CARTON (31722-437-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-438-30	31722-438	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	3 mg/1	1 BOTTLE in 1 CARTON (31722-438-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-439-30	31722-439	HUMAN PRESCRIPTION DRUG	Brexpiprazole	Brexpiprazole	TABLET, FILM COATED	ORAL	20231120	N/A	ANDA	ANDA213669	Camber Pharmaceuticals, Inc.	BREXPIPRAZOLE	4 mg/1	1 BOTTLE in 1 CARTON (31722-439-30) / 30 TABLET, FILM COATED in 1 BOTTLE