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)
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)
51407-882-90 51407-882 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20240401 N/A NDA AUTHORIZED GENERIC NDA020838 Golden State Medical Supply, Inc. CANDESARTAN CILEXETIL 4 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51407-882-90)
49884-658-09 49884-658 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20130521 20251231 NDA AUTHORIZED GENERIC NDA020838 Par Pharmaceutical Inc. CANDESARTAN CILEXETIL 4 mg/1 90 TABLET in 1 BOTTLE (49884-658-09)
63629-2126-1 63629-2126 HUMAN PRESCRIPTION DRUG Candesartan cilexetil Candesartan cilexetil TABLET ORAL 20210310 N/A NDA AUTHORIZED GENERIC NDA020838 Bryant Ranch Prepack CANDESARTAN CILEXETIL 4 mg/1 90 TABLET in 1 BOTTLE (63629-2126-1)
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