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"
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)
0615-8629-30 0615-8629 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20260414 N/A ANDA ANDA077095 NCS HealthCare of KY, LLC dba Vangard Labs METFORMIN HYDROCHLORIDE 500 mg/1 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8629-30) / 5 TABLET, FILM COATED in 1 BLISTER PACK
50090-7868-0 50090-7868 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20260129 N/A ANDA ANDA077095 A-S Medication Solutions METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7868-0)
0615-8578-05 0615-8578 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250417 N/A ANDA ANDA077095 NCS HealthCare of KY, LLC dba Vangard Labs METFORMIN HYDROCHLORIDE 1000 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8578-05)
0615-8578-39 0615-8578 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250417 N/A ANDA ANDA077095 NCS HealthCare of KY, LLC dba Vangard Labs METFORMIN HYDROCHLORIDE 1000 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8578-39)
0615-8629-39 0615-8629 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20260331 N/A ANDA ANDA077095 NCS HealthCare of KY, LLC dba Vangard Labs METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8629-39)
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)
65862-010-01 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)
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)
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)
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