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=NDA018998"
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
71205-075-90 71205-075 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20180702 N/A NDA AUTHORIZED GENERIC NDA018998 Proficient Rx LP ENALAPRIL MALEATE 10 mg/1 90 TABLET in 1 BOTTLE (71205-075-90)
71205-075-30 71205-075 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20180702 N/A NDA AUTHORIZED GENERIC NDA018998 Proficient Rx LP ENALAPRIL MALEATE 10 mg/1 30 TABLET in 1 BOTTLE (71205-075-30)
71205-075-60 71205-075 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20180702 N/A NDA AUTHORIZED GENERIC NDA018998 Proficient Rx LP ENALAPRIL MALEATE 10 mg/1 60 TABLET in 1 BOTTLE (71205-075-60)
71335-1141-1 71335-1141 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20220504 N/A NDA AUTHORIZED GENERIC NDA018998 Bryant Ranch Prepack ENALAPRIL MALEATE 2.5 mg/1 30 TABLET in 1 BOTTLE (71335-1141-1)
71335-1141-2 71335-1141 HUMAN PRESCRIPTION DRUG Enalapril Maleate Enalapril Maleate TABLET ORAL 20220504 N/A NDA AUTHORIZED GENERIC NDA018998 Bryant Ranch Prepack ENALAPRIL MALEATE 2.5 mg/1 90 TABLET in 1 BOTTLE (71335-1141-2)
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