药品注册申请号:204983
申请类型:ANDA (仿制药申请)
申请人:CHARTWELL RX
申请人全名:CHARTWELL RX SCIENCES LLC
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG No No AB 2023/01/05 2023/01/05 Discontinued
002 FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG No No AB 2023/01/05 Discontinued
批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期提交号审批结论申请内容分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2023/01/05 ORIG-1(原始申请) Approval STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
活性成分:FESOTERODINE FUMARATE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:4MG 治疗等效代码:AB
申请号产品号申请类型商品名活性成分剂型/给药途径规格市场状态RLDRSTE Code产品号批准日期申请人
022030 001 NDA TOVIAZ FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription Yes No AB 2008/10/31 PFIZER
204827 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2015/12/10 ALKEM LABS LTD
205007 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2017/02/17 AUROBINDO PHARMA
204946 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2017/10/03 ZYDUS PHARMS
204975 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2019/08/13 DR REDDYS
204973 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2023/01/04 ALEMBIC
204868 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Discontinued No No AB 2023/01/04 ACTAVIS LABS FL INC
204504 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2023/01/04 ANI PHARMS
205012 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Discontinued No No AB 2023/01/04 ACCORD HLTHCARE
205002 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2023/01/04 AMNEAL PHARMS NY
204983 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Discontinued No No AB 2023/01/05 CHARTWELL RX
204792 001 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 4MG Prescription No No AB 2024/01/09 HETERO LABS LTD V
活性成分:FESOTERODINE FUMARATE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:8MG 治疗等效代码:AB
申请号产品号申请类型商品名活性成分剂型/给药途径规格市场状态RLDRSTE Code产品号批准日期申请人
022030 002 NDA TOVIAZ FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription Yes Yes AB 2008/10/31 PFIZER
204827 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2015/12/10 ALKEM LABS LTD
205007 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2017/02/17 AUROBINDO PHARMA
204946 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2017/10/03 ZYDUS PHARMS
204975 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2019/08/13 DR REDDYS
204973 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2023/01/04 ALEMBIC
204868 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Discontinued No No AB 2023/01/04 ACTAVIS LABS FL INC
204504 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2023/01/04 ANI PHARMS
205012 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Discontinued No No AB 2023/01/04 ACCORD HLTHCARE
205002 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2023/01/04 AMNEAL PHARMS NY
204983 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Discontinued No No AB 2023/01/05 CHARTWELL RX
204792 002 ANDA FESOTERODINE FUMARATE FESOTERODINE FUMARATE TABLET, EXTENDED RELEASE;ORAL 8MG Prescription No No AB 2024/01/09 HETERO LABS LTD V
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