药品注册申请号:216548
申请类型:ANDA (仿制药申请)
申请人:RUBICON
申请人全名:RUBICON RESEARCH PRIVATE 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 DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 25MG No No AB 2023/05/11 2023/05/11 Prescription
002 DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG No No AB 2023/05/11 Prescription
003 DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG No No AB 2023/05/11 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
2024/11/21 SUPPL-4(补充) Approval Labeling STANDARD
2023/05/11 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:DICLOFENAC SODIUM 剂型/给药途径:TABLET, DELAYED RELEASE;ORAL 规格:25MG 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
075185 002 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 25MG Prescription No No AB 1998/11/13 CARLSBAD
090066 001 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 25MG Prescription No Yes AB 2010/12/01 UNIQUE
216548 001 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 25MG Prescription No No AB 2023/05/11 RUBICON
活性成分:DICLOFENAC SODIUM 剂型/给药途径:TABLET, DELAYED RELEASE;ORAL 规格:50MG 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
074514 001 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG Prescription No No AB 1996/03/26 ACTAVIS ELIZABETH
075185 003 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG Prescription No No AB 1998/11/13 CARLSBAD
090066 002 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG Prescription No Yes AB 2010/12/01 UNIQUE
216548 002 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 50MG Prescription No No AB 2023/05/11 RUBICON
活性成分:DICLOFENAC SODIUM 剂型/给药途径:TABLET, DELAYED RELEASE;ORAL 规格: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
074514 002 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG Prescription No No AB 1996/03/26 ACTAVIS ELIZABETH
075185 001 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG Prescription No No AB 1998/11/13 CARLSBAD
077863 003 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG Prescription No Yes AB 2007/06/08 UNIQUE
216548 003 ANDA DICLOFENAC SODIUM DICLOFENAC SODIUM TABLET, DELAYED RELEASE;ORAL 75MG Prescription No No AB 2023/05/11 RUBICON
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