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=ANDA209042"
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
67877-500-90 67877-500 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 20 mg/1 90 TABLET in 1 BOTTLE (67877-500-90)
67877-501-30 67877-501 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 30 TABLET in 1 BOTTLE (67877-501-30)
67877-501-90 67877-501 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 40 mg/1 90 TABLET in 1 BOTTLE (67877-501-90)
67877-502-30 67877-502 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 30 TABLET in 1 BOTTLE (67877-502-30)
67877-502-90 67877-502 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 40 mg/1 90 TABLET in 1 BOTTLE (67877-502-90)
67877-500-30 67877-500 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 10 mg/1; 20 mg/1 30 TABLET in 1 BOTTLE (67877-500-30)
67877-499-90 67877-499 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 90 TABLET in 1 BOTTLE (67877-499-90)
67877-499-30 67877-499 HUMAN PRESCRIPTION DRUG Amlodipine and olmesartan Medoxomil Amlodipine and olmesartan Medoxomil TABLET ORAL 20170814 N/A ANDA ANDA209042 Ascend Laboratories, LLC AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL 5 mg/1; 20 mg/1 30 TABLET in 1 BOTTLE (67877-499-30)
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