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
70771-1859-8	70771-1859	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70771-1859-8)
70771-1860-6	70771-1860	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70771-1860-6)
70771-1860-8	70771-1860	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70771-1860-8)
70771-1869-6	70771-1869	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70771-1869-6)
70771-1869-8	70771-1869	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70771-1869-8)
70771-1870-6	70771-1870	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70771-1870-6)
70771-1870-8	70771-1870	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70771-1870-8)
70771-1859-6	70771-1859	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70771-1859-6)
70710-1787-6	70710-1787	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70710-1787-6)
70710-1786-8	70710-1786	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70710-1786-8)
70710-1786-6	70710-1786	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70710-1786-6)
70710-1787-8	70710-1787	HUMAN PRESCRIPTION DRUG	ZITUVIMET	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70710-1787-8)
70710-1986-6	70710-1986	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70710-1986-6)
70710-1986-8	70710-1986	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70710-1986-8)
70710-1987-6	70710-1987	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70710-1987-6)
70710-1987-8	70710-1987	HUMAN PRESCRIPTION DRUG	Sitagliptin and metformin hydrochloride	Sitagliptin and Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240314	N/A	NDA AUTHORIZED GENERIC	NDA216743	Zydus Pharmaceuticals (USA) Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70710-1987-8)