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
17224-322-28	17224-322	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	METFORMIN HYDROCHLORIDE	TABLET, COATED	ORAL	20190501	N/A	ANDA	ANDA205096	Calvin Scott & Co., Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	28 TABLET, COATED in 1 BOTTLE (17224-322-28)
17224-322-30	17224-322	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	METFORMIN HYDROCHLORIDE	TABLET, COATED	ORAL	20190501	N/A	ANDA	ANDA205096	Calvin Scott & Co., Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, COATED in 1 BOTTLE (17224-322-30)
17224-322-56	17224-322	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	METFORMIN HYDROCHLORIDE	TABLET, COATED	ORAL	20190501	N/A	ANDA	ANDA205096	Calvin Scott & Co., Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	56 TABLET, COATED in 1 BOTTLE (17224-322-56)
17224-322-90	17224-322	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	METFORMIN HYDROCHLORIDE	TABLET, COATED	ORAL	20190501	N/A	ANDA	ANDA205096	Calvin Scott & Co., Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, COATED in 1 BOTTLE (17224-322-90)
69367-381-10	69367-381	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA205096	Westminster Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, COATED in 1 BOTTLE (69367-381-10)
69367-382-01	69367-382	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA205096	Westminster Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET, COATED in 1 BOTTLE (69367-382-01)
71335-2291-1	71335-2291	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20231201	N/A	ANDA	ANDA205096	Bryant Ranch Prepack	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, COATED in 1 BOTTLE (71335-2291-1)
70518-3212-0	70518-3212	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20210903	N/A	ANDA	ANDA205096	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-3212-0)
70518-3212-1	70518-3212	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20220706	N/A	ANDA	ANDA205096	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3212-1)
70518-3212-2	70518-3212	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20220717	N/A	ANDA	ANDA205096	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	1000 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3212-2)
70518-3611-0	70518-3611	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20230105	N/A	ANDA	ANDA205096	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, COATED in 1 BLISTER PACK (70518-3611-0)
70518-3611-1	70518-3611	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20230710	N/A	ANDA	ANDA205096	REMEDYREPACK INC.	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-3611-1)
51655-914-52	51655-914	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20230615	N/A	ANDA	ANDA205096	Northwind Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-914-52)