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
0378-8175-93	0378-8175	HUMAN PRESCRIPTION DRUG	Saxagliptin and Metformin	saxagliptin and metformin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230808	N/A	ANDA	ANDA205981	Mylan Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE	500 mg/1; 5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8175-93)
0378-8177-93	0378-8177	HUMAN PRESCRIPTION DRUG	Saxagliptin and Metformin	saxagliptin and metformin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230808	N/A	ANDA	ANDA205981	Mylan Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE	1000 mg/1; 5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8177-93)
0378-8176-91	0378-8176	HUMAN PRESCRIPTION DRUG	Saxagliptin and Metformin	saxagliptin and metformin	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230808	N/A	ANDA	ANDA205981	Mylan Pharmaceuticals Inc.	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE	1000 mg/1; 2.5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-8176-91)