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
68462-726-05	68462-726	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-726-05)
68462-726-30	68462-726	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-726-30)
68462-726-90	68462-726	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-726-90)
68462-727-05	68462-727	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-727-05)
68462-727-14	68462-727	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (68462-727-14) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-727-30	68462-727	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-727-30)
68462-727-90	68462-727	HUMAN PRESCRIPTION DRUG	SAXAGLIPTIN	SAXAGLIPTIN	TABLET, FILM COATED	ORAL	20230731	N/A	ANDA	ANDA205994	Glenmark Pharmaceuticals Inc., USA	SAXAGLIPTIN HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-727-90)