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=NDA020838"
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
72162-1510-9 72162-1510 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20230829 N/A NDA AUTHORIZED GENERIC NDA020838 Bryant Ranch Prepack CANDESARTAN CILEXETIL 4 mg/1 90 TABLET in 1 BOTTLE (72162-1510-9)
72162-1511-9 72162-1511 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20230829 N/A NDA AUTHORIZED GENERIC NDA020838 Bryant Ranch Prepack CANDESARTAN CILEXETIL 8 mg/1 90 TABLET in 1 BOTTLE (72162-1511-9)
62559-688-99 62559-688 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20240315 N/A NDA AUTHORIZED GENERIC NDA020838 ANI Pharmaceuticals, Inc. CANDESARTAN CILEXETIL 16 mg/1 50000 TABLET in 1 BOX (62559-688-99)
62559-687-99 62559-687 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20240315 N/A NDA AUTHORIZED GENERIC NDA020838 ANI Pharmaceuticals, Inc. CANDESARTAN CILEXETIL 8 mg/1 50000 TABLET in 1 BOX (62559-687-99)
62559-686-99 62559-686 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20240315 N/A NDA AUTHORIZED GENERIC NDA020838 ANI Pharmaceuticals, Inc. CANDESARTAN CILEXETIL 4 mg/1 50000 TABLET in 1 BOX (62559-686-99)
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