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
53002-4251-0	53002-4251	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-4251-0)
53002-4251-3	53002-4251	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-4251-3)
53002-4251-6	53002-4251	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-4251-6)
53002-4445-0	53002-4445	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (53002-4445-0)
53002-4445-3	53002-4445	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-4445-3)
53002-4445-6	53002-4445	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20240101	N/A	ANDA	ANDA077095	RPK Pharmaceuticals, Inc.	METFORMIN HYDROCHLORIDE	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-4445-6)
50090-6485-0	50090-6485	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20230517	N/A	ANDA	ANDA077095	A-S Medication Solutions	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6485-0)
65862-008-01	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-008-01)
65862-008-05	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-008-05)
65862-008-33	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (65862-008-33)
65862-008-45	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	4500 TABLET, FILM COATED in 1 BOTTLE (65862-008-45)
65862-008-50	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (65862-008-50)
65862-008-60	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (65862-008-60)
65862-008-90	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-008-90)
65862-008-99	65862-008	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-008-99)
65862-009-01	65862-009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	850 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-009-01)
65862-009-05	65862-009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	850 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-009-05)
65862-009-33	65862-009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	850 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (65862-009-33)
65862-009-44	65862-009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	850 mg/1	2500 TABLET, FILM COATED in 1 BOTTLE (65862-009-44)
65862-009-50	65862-009	HUMAN PRESCRIPTION DRUG	Metformin Hydrochloride	Metformin Hydrochloride	TABLET, FILM COATED	ORAL	20050114	N/A	ANDA	ANDA077095	Aurobindo Pharma Limited	METFORMIN HYDROCHLORIDE	850 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (65862-009-50)