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=NDA021228"
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
0009-5190-01 0009-5190 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20000222 20241231 NDA NDA021228 Pharmacia and Upjohn Company LLC TOLTERODINE TARTRATE 2 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5190-01)
0009-5190-02 0009-5190 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20000222 20241231 NDA NDA021228 Pharmacia and Upjohn Company LLC TOLTERODINE TARTRATE 2 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5190-02)
0009-5190-03 0009-5190 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20000222 20240831 NDA NDA021228 Pharmacia and Upjohn Company LLC TOLTERODINE TARTRATE 2 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5190-03)
0009-5191-01 0009-5191 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20000222 20241130 NDA NDA021228 Pharmacia and Upjohn Company LLC TOLTERODINE TARTRATE 4 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5191-01)
0009-5191-02 0009-5191 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20000222 20241231 NDA NDA021228 Pharmacia and Upjohn Company LLC TOLTERODINE TARTRATE 4 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5191-02)
58151-103-77 58151-103 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20240110 N/A NDA NDA021228 Viatris Specialty LLC TOLTERODINE TARTRATE 2 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-103-77)
58151-103-93 58151-103 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20240110 N/A NDA NDA021228 Viatris Specialty LLC TOLTERODINE TARTRATE 2 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-103-93)
58151-104-77 58151-104 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20240320 N/A NDA NDA021228 Viatris Specialty LLC TOLTERODINE TARTRATE 4 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-104-77)
58151-104-93 58151-104 HUMAN PRESCRIPTION DRUG Detrol LA tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20240320 N/A NDA NDA021228 Viatris Specialty LLC TOLTERODINE TARTRATE 4 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-104-93)
59762-0047-1 59762-0047 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20160122 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 2 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0047-1)
59762-0047-2 59762-0047 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20160122 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 2 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0047-2)
59762-0047-3 59762-0047 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20160122 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 2 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0047-3)
59762-0048-1 59762-0048 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20141230 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 4 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0048-1)
59762-0048-2 59762-0048 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20141230 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 4 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0048-2)
59762-0048-3 59762-0048 HUMAN PRESCRIPTION DRUG Tolterodine Tartrate Extended Release tolterodine tartrate CAPSULE, EXTENDED RELEASE ORAL 20141230 N/A NDA AUTHORIZED GENERIC NDA021228 Greenstone LLC TOLTERODINE TARTRATE 4 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (59762-0048-3)
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