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
65841-027-01	65841-027	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20050928	N/A	ANDA	ANDA077060	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-027-01)
65841-027-05	65841-027	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20050928	N/A	ANDA	ANDA077060	Zydus Lifesciences Limited	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-027-05)
72578-035-01	72578-035	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190315	N/A	ANDA	ANDA077060	Viona Pharmaceuticals Inc	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-035-01)
72578-035-05	72578-035	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190315	N/A	ANDA	ANDA077060	Viona Pharmaceuticals Inc	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-035-05)