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=ANDA206763"
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
67877-445-30 67877-445 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, COATED ORAL 20170424 N/A ANDA ANDA206763 Ascend Laboratories, LLC OLMESARTAN MEDOXOMIL 5 mg/1 30 TABLET, COATED in 1 BOTTLE (67877-445-30)
67877-445-10 67877-445 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, COATED ORAL 20170424 N/A ANDA ANDA206763 Ascend Laboratories, LLC OLMESARTAN MEDOXOMIL 5 mg/1 1000 TABLET, COATED in 1 BOTTLE (67877-445-10)
67877-445-05 67877-445 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, COATED ORAL 20170424 N/A ANDA ANDA206763 Ascend Laboratories, LLC OLMESARTAN MEDOXOMIL 5 mg/1 500 TABLET, COATED in 1 BOTTLE (67877-445-05)
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