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
42806-632-01	42806-632	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-632-01)
42806-632-05	42806-632	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-632-05)
42806-632-10	42806-632	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-632-10)
42806-633-01	42806-633	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-633-01)
42806-633-05	42806-633	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	750 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-633-05)
42806-633-10	42806-633	HUMAN PRESCRIPTION DRUG	METFORMIN HYDROCHLORIDE	METFORMIN HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA211052	Epic Pharma, LLC	METFORMIN HYDROCHLORIDE	750 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-633-10)