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=NDA018225"
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
42799-121-01 42799-121 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20151015 N/A NDA AUTHORIZED GENERIC NDA018225 Edenbridge Pharmaceuticals LLC. BUMETANIDE 2 mg/1 100 TABLET in 1 BOTTLE (42799-121-01)
42799-121-02 42799-121 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20151015 N/A NDA AUTHORIZED GENERIC NDA018225 Edenbridge Pharmaceuticals LLC. BUMETANIDE 2 mg/1 500 TABLET in 1 BOTTLE (42799-121-02)
42799-120-02 42799-120 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20151015 N/A NDA AUTHORIZED GENERIC NDA018225 Edenbridge Pharmaceuticals LLC. BUMETANIDE 1 mg/1 500 TABLET in 1 BOTTLE (42799-120-02)
42799-120-01 42799-120 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20151015 N/A NDA AUTHORIZED GENERIC NDA018225 Edenbridge Pharmaceuticals LLC. BUMETANIDE 1 mg/1 100 TABLET in 1 BOTTLE (42799-120-01)
42799-119-01 42799-119 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20151015 N/A NDA AUTHORIZED GENERIC NDA018225 Edenbridge Pharmaceuticals LLC. BUMETANIDE .5 mg/1 100 TABLET in 1 BOTTLE (42799-119-01)
60687-384-01 60687-384 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20200713 N/A NDA AUTHORIZED GENERIC NDA018225 American Health Packaging BUMETANIDE 1 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
60687-384-65 60687-384 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20230605 N/A NDA AUTHORIZED GENERIC NDA018225 American Health Packaging BUMETANIDE 1 mg/1 50 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
60687-535-65 60687-535 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20240901 N/A NDA AUTHORIZED GENERIC NDA018225 American Health Packaging BUMETANIDE 2 mg/1 50 BLISTER PACK in 1 CARTON (60687-535-65) / 1 TABLET in 1 BLISTER PACK (60687-535-11)
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