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
70710-1806-3	70710-1806	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1806-3)
70710-2037-6	70710-2037	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2037-6)
70710-2038-3	70710-2038	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2038-3)
70710-2036-6	70710-2036	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2036-6)
70710-1805-6	70710-1805	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1805-6)
70710-1804-6	70710-1804	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Pharmaceuticals USA Inc.	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1804-6)
70771-1879-6	70771-1879	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1879-6)
70771-1887-6	70771-1887	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	500 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1887-6)
70771-1880-6	70771-1880	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1880-6)
70771-1881-3	70771-1881	HUMAN PRESCRIPTION DRUG	ZITUVIMET XR	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1881-3)
70771-1886-6	70771-1886	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 50 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1886-6)
70771-1888-3	70771-1888	HUMAN PRESCRIPTION DRUG	Sitagliptin and Metformin Hydrochloride	sitagliptin and metformin hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20241031	N/A	NDA AUTHORIZED GENERIC	NDA216778	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE; SITAGLIPTIN	1000 mg/1; 100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1888-3)