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=ANDA203820"
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
72162-2558-1 72162-2558 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20251104 N/A ANDA ANDA203820 Bryant Ranch Prepack REPAGLINIDE 1 mg/1 100 TABLET in 1 BOTTLE (72162-2558-1)
57237-159-01 57237-159 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE 2 mg/1 100 TABLET in 1 BOTTLE (57237-159-01)
57237-159-05 57237-159 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE 2 mg/1 500 TABLET in 1 BOTTLE (57237-159-05)
65862-671-01 65862-671 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 1 mg/1 100 TABLET in 1 BOTTLE (65862-671-01)
65862-671-05 65862-671 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 1 mg/1 500 TABLET in 1 BOTTLE (65862-671-05)
65862-671-99 65862-671 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 1 mg/1 1000 TABLET in 1 BOTTLE (65862-671-99)
57237-157-01 57237-157 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE .5 mg/1 100 TABLET in 1 BOTTLE (57237-157-01)
57237-157-05 57237-157 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE .5 mg/1 500 TABLET in 1 BOTTLE (57237-157-05)
65862-672-01 65862-672 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 2 mg/1 100 TABLET in 1 BOTTLE (65862-672-01)
65862-672-05 65862-672 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 2 mg/1 500 TABLET in 1 BOTTLE (65862-672-05)
65862-672-99 65862-672 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE 2 mg/1 1000 TABLET in 1 BOTTLE (65862-672-99)
60687-560-21 60687-560 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20200917 N/A ANDA ANDA203820 American Health Packaging REPAGLINIDE 1 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-560-21) / 1 TABLET in 1 BLISTER PACK (60687-560-11)
57237-158-01 57237-158 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE 1 mg/1 100 TABLET in 1 BOTTLE (57237-158-01)
57237-158-05 57237-158 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Rising Pharma Holdings, Inc. REPAGLINIDE 1 mg/1 500 TABLET in 1 BOTTLE (57237-158-05)
65862-670-01 65862-670 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE .5 mg/1 100 TABLET in 1 BOTTLE (65862-670-01)
65862-670-05 65862-670 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE .5 mg/1 500 TABLET in 1 BOTTLE (65862-670-05)
65862-670-99 65862-670 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20140122 N/A ANDA ANDA203820 Aurobindo Pharma Limited REPAGLINIDE .5 mg/1 1000 TABLET in 1 BOTTLE (65862-670-99)
63629-4866-1 63629-4866 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20250116 N/A ANDA ANDA203820 Bryant Ranch Prepack REPAGLINIDE .5 mg/1 30 TABLET in 1 BOTTLE (63629-4866-1)
63629-4866-2 63629-4866 HUMAN PRESCRIPTION DRUG Repaglinide Repaglinide TABLET ORAL 20250116 N/A ANDA ANDA203820 Bryant Ranch Prepack REPAGLINIDE .5 mg/1 90 TABLET in 1 BOTTLE (63629-4866-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase