美国药品NDC数据库(National Drug Code Database)=>当前查询条件:"申请号:NDA020771;",共 5 条结果。点击左侧“产品NDC”可以查询指定剂量规格药品的所有包装规格及药品说明书。
产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 市场分类 申请号 标签持有者 活性成分 规格 规格单位
0009-4541HUMAN PRESCRIPTION DRUGDetroltolterodine tartrateTABLET, FILM COATEDORAL19980325NDANDA020771Pharmacia and Upjohn Company LLCTOLTERODINE TARTRATE1mg/1
0009-4544HUMAN PRESCRIPTION DRUGDetroltolterodine tartrateTABLET, FILM COATEDORAL19980325NDANDA020771Pharmacia and Upjohn Company LLCTOLTERODINE TARTRATE2mg/1
59762-0170HUMAN PRESCRIPTION DRUGTolterodine TartrateTolterodine TartrateTABLET, FILM COATEDORAL20140121NDA AUTHORIZED GENERICNDA020771Greenstone LLCTOLTERODINE TARTRATE1mg/1
59762-0800HUMAN PRESCRIPTION DRUGTolterodine TartrateTolterodine TartrateTABLET, FILM COATEDORAL20140121NDA AUTHORIZED GENERICNDA020771Greenstone LLCTOLTERODINE TARTRATE2mg/1
70518-1416HUMAN PRESCRIPTION DRUGTolterodine TartrateTolterodine TartrateTABLET, FILM COATEDORAL20180917NDA AUTHORIZED GENERICNDA020771REMEDYREPACK INC.TOLTERODINE TARTRATE2mg/1