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
0310-6105-90	0310-6105	HUMAN PRESCRIPTION DRUG	ONGLYZA	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20141219	N/A	NDA	NDA022350	AstraZeneca Pharmaceuticals LP	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0310-6105-90)
0310-6105-30	0310-6105	HUMAN PRESCRIPTION DRUG	ONGLYZA	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20141218	N/A	NDA	NDA022350	AstraZeneca Pharmaceuticals LP	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0310-6105-30)
0310-6100-90	0310-6100	HUMAN PRESCRIPTION DRUG	ONGLYZA	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20150106	N/A	NDA	NDA022350	AstraZeneca Pharmaceuticals LP	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0310-6100-90)
0310-6100-30	0310-6100	HUMAN PRESCRIPTION DRUG	ONGLYZA	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20141121	N/A	NDA	NDA022350	AstraZeneca Pharmaceuticals LP	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0310-6100-30)
55154-6931-2	55154-6931	HUMAN PRESCRIPTION DRUG	ONGLYZA	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20141120	N/A	NDA	NDA022350	Cardinal Health 107, LLC	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	1080 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6931-2)