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 102 条，共 6 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
63187-239-90 63187-239 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA077095 Proficient Rx LP METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-239-90)
71610-929-30 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71610-929-30)
71610-929-53 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-929-53)
71610-929-60 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-929-60)
71610-929-70 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-929-70)
71610-929-80 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-929-80)
71610-929-94 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 360 TABLET, FILM COATED in 1 BOTTLE (71610-929-94)
59651-854-01 59651-854 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20240329 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-854-01)
59651-854-05 59651-854 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20240329 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-854-05)
59651-854-45 59651-854 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20240329 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 4500 TABLET, FILM COATED in 1 BOTTLE (59651-854-45)
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)
71610-941-60 71610-941 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250825 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-941-60)
71610-941-80 71610-941 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250825 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-941-80)
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)
70518-1149-0 70518-1149 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20180501 N/A ANDA ANDA077095 REMEDYREPACK INC. METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1149-0)
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)
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