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
0781-5802-60	0781-5802	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0781-5802-60)
0781-5802-71	0781-5802	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	1000 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (0781-5802-71)
0781-5802-73	0781-5802	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	1000 mg/1; 50 mg/1	350 TABLET, FILM COATED in 1 BOTTLE (0781-5802-73)
0781-5801-05	0781-5801	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	500 mg/1; 50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0781-5801-05)
0781-5801-60	0781-5801	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	500 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0781-5801-60)
0781-5801-71	0781-5801	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20251202	N/A	ANDA	ANDA202388	Sandoz Inc	METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE	500 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (0781-5801-71)