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
83301-0009-2	83301-0009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240101	N/A	ANDA	ANDA205096	Mullan Pharmaceutical Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	500 TABLET, COATED in 1 BOTTLE (83301-0009-2)
83301-0009-3	83301-0009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240101	N/A	ANDA	ANDA205096	Mullan Pharmaceutical Inc.	METFORMIN HYDROCHLORIDE	850 mg/1	1000 TABLET, COATED in 1 BOTTLE (83301-0009-3)
83301-0010-1	83301-0010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240101	N/A	ANDA	ANDA205096	Mullan Pharmaceutical Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, COATED in 1 BOTTLE (83301-0010-1)
83301-0010-2	83301-0010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240101	N/A	ANDA	ANDA205096	Mullan Pharmaceutical Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, COATED in 1 BOTTLE (83301-0010-2)
83301-0010-3	83301-0010	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240101	N/A	ANDA	ANDA205096	Mullan Pharmaceutical Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, COATED in 1 BOTTLE (83301-0010-3)
69367-381-01	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	100 TABLET, COATED in 1 BOTTLE (69367-381-01)
69367-381-05	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	500 TABLET, COATED in 1 BOTTLE (69367-381-05)
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)
69367-382-05	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	500 TABLET, COATED in 1 BOTTLE (69367-382-05)
69367-382-10	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	1000 TABLET, COATED in 1 BOTTLE (69367-382-10)
69367-383-01	69367-383	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA205096	Westminster Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, COATED in 1 BOTTLE (69367-383-01)
69367-383-05	69367-383	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA205096	Westminster Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	500 TABLET, COATED in 1 BOTTLE (69367-383-05)
69367-383-10	69367-383	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, COATED	ORAL	20240304	N/A	ANDA	ANDA205096	Westminster Pharmaceuticals, LLC	METFORMIN HYDROCHLORIDE	1000 mg/1	1000 TABLET, COATED in 1 BOTTLE (69367-383-10)