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=NDA020771"
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
58151-099-91 58151-099 HUMAN PRESCRIPTION DRUG Detrol tolterodine tartrate TABLET, FILM COATED ORAL 20240801 N/A NDA NDA020771 Viatris Specialty LLC TOLTERODINE TARTRATE 2 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (58151-099-91)
58151-098-91 58151-098 HUMAN PRESCRIPTION DRUG Detrol tolterodine tartrate TABLET, FILM COATED ORAL 20240521 N/A NDA NDA020771 Viatris Specialty LLC TOLTERODINE TARTRATE 1 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (58151-098-91)
0009-4544-02 0009-4544 HUMAN PRESCRIPTION DRUG Detrol tolterodine tartrate TABLET, FILM COATED ORAL 19980325 20251231 NDA NDA020771 PHARMACIA & UPJOHN COMPANY LLC TOLTERODINE TARTRATE 2 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0009-4544-02)
59762-0800-2 59762-0800 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Tolterodine Tartrate TABLET, FILM COATED ORAL 20140121 N/A NDA AUTHORIZED GENERIC NDA020771 Greenstone LLC TOLTERODINE TARTRATE 2 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (59762-0800-2)
59762-0800-6 59762-0800 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Tolterodine Tartrate TABLET, FILM COATED ORAL 20140121 N/A NDA AUTHORIZED GENERIC NDA020771 Greenstone LLC TOLTERODINE TARTRATE 2 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59762-0800-6)
0009-4541-02 0009-4541 HUMAN PRESCRIPTION DRUG Detrol tolterodine tartrate TABLET, FILM COATED ORAL 19980325 20241231 NDA NDA020771 PHARMACIA & UPJOHN COMPANY LLC TOLTERODINE TARTRATE 1 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0009-4541-02)
59762-0170-1 59762-0170 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Tolterodine Tartrate TABLET, FILM COATED ORAL 20140121 N/A NDA AUTHORIZED GENERIC NDA020771 Greenstone LLC TOLTERODINE TARTRATE 1 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59762-0170-1)
59762-0170-6 59762-0170 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Tolterodine Tartrate TABLET, FILM COATED ORAL 20140121 N/A NDA AUTHORIZED GENERIC NDA020771 Greenstone LLC TOLTERODINE TARTRATE 1 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (59762-0170-6)
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