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=ANDA213329"
符合检索条件的记录共 5 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
69097-999-07 69097-999 HUMAN PRESCRIPTION DRUG Phytonadione Phytonadione TABLET ORAL 20231201 N/A ANDA ANDA213329 Cipla USA., Inc. PHYTONADIONE 5 mg/1 100 TABLET in 1 BOTTLE (69097-999-07)
69097-999-02 69097-999 HUMAN PRESCRIPTION DRUG Phytonadione Phytonadione TABLET ORAL 20231201 N/A ANDA ANDA213329 Cipla USA., Inc. PHYTONADIONE 5 mg/1 30 TABLET in 1 BOTTLE (69097-999-02)
76282-740-30 76282-740 HUMAN PRESCRIPTION DRUG Phytonadione Phytonadione TABLET ORAL 20231201 N/A ANDA ANDA213329 Exelan Pharmaceuticals, Inc. PHYTONADIONE 5 mg/1 1 BOTTLE in 1 CARTON (76282-740-30) / 30 TABLET in 1 BOTTLE
50228-333-01 50228-333 HUMAN PRESCRIPTION DRUG Phytonadione Phytonadione TABLET ORAL 20230728 N/A ANDA ANDA213329 ScieGen Pharmaceuticals Inc PHYTONADIONE 5 mg/1 1 BOTTLE in 1 CARTON (50228-333-01) / 100 TABLET in 1 BOTTLE
50228-333-30 50228-333 HUMAN PRESCRIPTION DRUG Phytonadione Phytonadione TABLET ORAL 20230728 N/A ANDA ANDA213329 ScieGen Pharmaceuticals Inc PHYTONADIONE 5 mg/1 1 BOTTLE in 1 CARTON (50228-333-30) / 30 TABLET in 1 BOTTLE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase