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=ANDA209333"
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
71205-583-30 71205-583 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210625 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-583-30)
71205-583-60 71205-583 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210625 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-583-60)
71205-583-90 71205-583 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210625 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-583-90)
71205-559-30 71205-559 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210505 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-559-30)
71205-559-60 71205-559 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210505 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-559-60)
71205-559-90 71205-559 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20210505 N/A ANDA ANDA209333 Proficient Rx LP SOLIFENACIN SUCCINATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-559-90)
67184-0517-1 67184-0517 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate Tablets TABLET, FILM COATED ORAL 20200401 N/A ANDA ANDA209333 Qilu Pharmaceutical Co., Ltd. SOLIFENACIN SUCCINATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67184-0517-1)
67184-0517-2 67184-0517 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate Tablets TABLET, FILM COATED ORAL 20200401 N/A ANDA ANDA209333 Qilu Pharmaceutical Co., Ltd. SOLIFENACIN SUCCINATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (67184-0517-2)
67184-0517-3 67184-0517 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate Tablets TABLET, FILM COATED ORAL 20200401 N/A ANDA ANDA209333 Qilu Pharmaceutical Co., Ltd. SOLIFENACIN SUCCINATE 10 mg/1 2000 TABLET, FILM COATED in 1 BOTTLE (67184-0517-3)
67184-0517-4 67184-0517 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate Tablets TABLET, FILM COATED ORAL 20200401 N/A ANDA ANDA209333 Qilu Pharmaceutical Co., Ltd. SOLIFENACIN SUCCINATE 10 mg/1 40 TABLET, FILM COATED in 1 BLISTER PACK (67184-0517-4)
60505-4702-3 60505-4702 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20190520 N/A ANDA ANDA209333 Apotex Corp. SOLIFENACIN SUCCINATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-4702-3)
60505-4703-3 60505-4703 HUMAN PRESCRIPTION DRUG Solifenacin Succinate Solifenacin Succinate TABLET, FILM COATED ORAL 20190520 N/A ANDA ANDA209333 Apotex Corp. SOLIFENACIN SUCCINATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-4703-3)
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