药品注册申请号：203354
申请类型：ANDA (仿制药申请)
申请人：DR REDDYS
申请人全名：DR REDDYS LABORATORIES LTD
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 PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG No Yes AB 2015/08/07 2015/08/07 Prescription
002 PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG No No AB 2015/08/07 Prescription
003 PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG No No AB 2015/08/07 Prescription
004 PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG No No AB 2015/08/07 Prescription
005 PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG No No AB 2015/08/07 Prescription
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
2020/10/14 SUPPL-6（补充） Approval Labeling STANDARD
2020/10/14 SUPPL-5（补充） Approval Labeling STANDARD
2020/10/14 SUPPL-2（补充） Approval Labeling STANDARD
2016/06/24 SUPPL-1（补充） Approval Labeling STANDARD
2015/08/07 ORIG-1（原始申请） Approval
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
无
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
无
与本品治疗等效的药品
活性成分:PRAMIPEXOLE DIHYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:0.375MG 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
022421 001 NDA MIRAPEX ER PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Discontinued Yes No AB 2010/02/19 BOEHRINGER INGELHEIM
202206 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Discontinued No No AB 2014/02/06 ENDO OPERATIONS
202353 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2014/12/04 SANDOZ
203354 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No Yes AB 2015/08/07 DR REDDYS
201963 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2016/04/21 ACTAVIS ELIZABETH
206156 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2016/06/24 MACLEODS PHARMS LTD
202891 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2017/12/12 ZYDUS PHARMS
204518 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2019/01/02 ALEMBIC
212797 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2021/06/11 XIAMEN LP PHARM CO
213444 001 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.375MG Prescription No No AB 2022/02/03 NOVAST LABS
活性成分:PRAMIPEXOLE DIHYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:0.75MG 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
022421 002 NDA MIRAPEX ER PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Discontinued Yes No AB 2010/02/19 BOEHRINGER INGELHEIM
202206 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Discontinued No No AB 2014/02/06 ENDO OPERATIONS
202353 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2014/12/04 SANDOZ
203354 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2015/08/07 DR REDDYS
201963 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2016/04/21 ACTAVIS ELIZABETH
206156 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2016/06/24 MACLEODS PHARMS LTD
202891 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2017/12/12 ZYDUS PHARMS
204518 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2019/01/02 ALEMBIC
212797 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2021/06/11 XIAMEN LP PHARM CO
213444 002 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 0.75MG Prescription No No AB 2022/02/03 NOVAST LABS
活性成分:PRAMIPEXOLE DIHYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:1.5MG 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
022421 003 NDA MIRAPEX ER PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Discontinued Yes No AB 2010/02/19 BOEHRINGER INGELHEIM
202206 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Discontinued No No AB 2014/02/06 ENDO OPERATIONS
202353 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2014/12/04 SANDOZ
203354 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2015/08/07 DR REDDYS
201963 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2016/04/21 ACTAVIS ELIZABETH
206156 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2016/06/24 MACLEODS PHARMS LTD
202891 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2017/12/12 ZYDUS PHARMS
204518 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2019/01/02 ALEMBIC
213444 003 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.5MG Prescription No No AB 2022/02/03 NOVAST LABS
活性成分:PRAMIPEXOLE DIHYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:3MG 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
022421 004 NDA MIRAPEX ER PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Discontinued Yes No AB 2010/02/19 BOEHRINGER INGELHEIM
202206 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Discontinued No No AB 2014/02/06 ENDO OPERATIONS
202353 004 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2014/12/04 SANDOZ
203354 004 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2015/08/07 DR REDDYS
201963 004 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2016/04/21 ACTAVIS ELIZABETH
206156 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2016/06/24 MACLEODS PHARMS LTD
202891 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2017/12/12 ZYDUS PHARMS
204518 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2019/01/02 ALEMBIC
213444 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 3MG Prescription No No AB 2022/02/03 NOVAST LABS
活性成分:PRAMIPEXOLE DIHYDROCHLORIDE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:4.5MG 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
022421 005 NDA MIRAPEX ER PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Discontinued Yes No AB 2010/02/19 BOEHRINGER INGELHEIM
202206 007 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Discontinued No No AB 2014/02/06 ENDO OPERATIONS
202353 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2014/12/04 SANDOZ
203354 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2015/08/07 DR REDDYS
201963 005 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2016/04/21 ACTAVIS ELIZABETH
206156 006 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2016/06/24 MACLEODS PHARMS LTD
202891 007 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2017/12/12 ZYDUS PHARMS
204518 007 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2019/01/02 ALEMBIC
213444 007 ANDA PRAMIPEXOLE DIHYDROCHLORIDE PRAMIPEXOLE DIHYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 4.5MG Prescription No No AB 2022/02/03 NOVAST LABS
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