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
65862-825-90	65862-825	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-825-90)
65862-826-01	65862-826	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-826-01)
65862-826-05	65862-826	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-826-05)
65862-826-30	65862-826	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-826-30)
65862-826-90	65862-826	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-826-90)
65862-825-30	65862-825	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-825-30)
65862-825-05	65862-825	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-825-05)
65862-825-01	65862-825	HUMAN PRESCRIPTION DRUG	Saxagliptin	Saxagliptin	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205972	Aurobindo Pharma Limited	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-825-01)