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
0310-6125-60	0310-6125	HUMAN PRESCRIPTION DRUG	KOMBIGLYZE XR	SAXAGLIPTIN AND METFORMIN HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141204	N/A	NDA	NDA200678	AstraZeneca Pharmaceuticals LP	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE	1000 mg/1; 2.5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0310-6125-60)
0310-6145-30	0310-6145	HUMAN PRESCRIPTION DRUG	KOMBIGLYZE XR	SAXAGLIPTIN AND METFORMIN HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20141222	N/A	NDA	NDA200678	AstraZeneca Pharmaceuticals LP	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE	1000 mg/1; 5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0310-6145-30)
0310-6135-30	0310-6135	HUMAN PRESCRIPTION DRUG	KOMBIGLYZE XR	SAXAGLIPTIN AND METFORMIN HYDROCHLORIDE	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20150101	N/A	NDA	NDA200678	AstraZeneca Pharmaceuticals LP	METFORMIN HYDROCHLORIDE; SAXAGLIPTIN HYDROCHLORIDE	500 mg/1; 5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0310-6135-30)