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
42806-405-60	42806-405	HUMAN PRESCRIPTION DRUG	metformin hydrochloride	metformin hydrochloride tablets	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190104	N/A	ANDA	ANDA209993	EPIC PHARMA, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-405-60)
42806-406-60	42806-406	HUMAN PRESCRIPTION DRUG	metformin hydrochloride	metformin hydrochloride tablet	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190104	N/A	ANDA	ANDA209993	EPIC PHARMA, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-406-60)
70247-018-60	70247-018	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride Extended-Release Tablets	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190301	N/A	ANDA	ANDA209993	Qingdao BAHEAL Pharmaceutical Co., Ltd.	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70247-018-60)
70247-019-60	70247-019	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride Extended-Release Tablets	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190301	N/A	ANDA	ANDA209993	Qingdao BAHEAL Pharmaceutical Co., Ltd.	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70247-019-60)