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）
检索条件:" 注册申请号=ANDA077095"
符合检索条件的记录共 88 条，共 5 页，当前第 2 页 ，可点击列名称排序
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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
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)
65862-009-60 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 60 TABLET, FILM COATED in 1 BOTTLE (65862-009-60)
65862-009-90 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 90 TABLET, FILM COATED in 1 BOTTLE (65862-009-90)
65862-009-99 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 1000 TABLET, FILM COATED in 1 BOTTLE (65862-009-99)
65862-010-01 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-010-01)
65862-010-05 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-010-05)
65862-010-33 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 300 TABLET, FILM COATED in 1 BOTTLE (65862-010-33)
65862-010-46 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 2000 TABLET, FILM COATED in 1 BOTTLE (65862-010-46)
65862-010-50 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (65862-010-50)
65862-010-60 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-010-60)
65862-010-90 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-010-90)
65862-010-99 65862-010 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 1000 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-010-99)
51655-649-25 51655-649 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250723 N/A ANDA ANDA077095 Northwind Health Company, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-25)
51655-649-26 51655-649 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20230623 N/A ANDA ANDA077095 Northwind Health Company, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)
51655-649-52 51655-649 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20210401 N/A ANDA ANDA077095 Northwind Health Company, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)
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