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
45802-169-72	45802-169	HUMAN PRESCRIPTION DRUG	alogliptin and metformin hydrochloride	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20160408	N/A	NDA AUTHORIZED GENERIC	NDA203414	Padagis Israel Pharmaceuticals Ltd	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (45802-169-72)
45802-211-72	45802-211	HUMAN PRESCRIPTION DRUG	alogliptin and metformin hydrochloride	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20160408	N/A	NDA AUTHORIZED GENERIC	NDA203414	Padagis Israel Pharmaceuticals Ltd	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (45802-211-72)
64764-335-01	64764-335	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 500 mg/1	4 CARTON in 1 TRAY (64764-335-01) / 1 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK
64764-335-60	64764-335	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64764-335-60)
64764-335-77	64764-335	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (64764-335-77)
64764-335-80	64764-335	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 500 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (64764-335-80)
64764-337-01	64764-337	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	4 CARTON in 1 TRAY (64764-337-01) / 1 BLISTER PACK in 1 CARTON / 14 TABLET, FILM COATED in 1 BLISTER PACK
64764-337-60	64764-337	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64764-337-60)
64764-337-77	64764-337	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (64764-337-77)
64764-337-80	64764-337	HUMAN PRESCRIPTION DRUG	KAZANO	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20130125	N/A	NDA	NDA203414	Takeda Pharmaceuticals America, Inc.	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (64764-337-80)
50090-5993-0	50090-5993	HUMAN PRESCRIPTION DRUG	alogliptin and metformin hydrochloride	alogliptin and metformin hydrochloride	TABLET, FILM COATED	ORAL	20220610	N/A	NDA AUTHORIZED GENERIC	NDA203414	A-S Medication Solutions	ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE	12.5 mg/1; 1000 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5993-0)