药品注册申请号:075229
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 POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG No No AB 1998/11/20 1998/11/20 Prescription
002 DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 25MG No No AB 2021/09/16 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-35(补充) Approval Labeling STANDARD
2021/04/28 SUPPL-23(补充) Approval Labeling STANDARD
2021/04/26 SUPPL-20(补充) Approval Labeling STANDARD
2014/12/06 SUPPL-16(补充) Approval Labeling
2009/09/04 SUPPL-14(补充) Approval Labeling
2008/04/29 SUPPL-12(补充) Approval Labeling
2006/10/05 SUPPL-11(补充) Approval Labeling
2002/10/02 SUPPL-5(补充) Approval Manufacturing (CMC)
2002/10/02 SUPPL-4(补充) Approval Manufacturing (CMC)
2002/10/02 SUPPL-3(补充) Approval Manufacturing (CMC)
2002/09/10 SUPPL-6(补充) Approval Labeling
2002/03/18 SUPPL-2(补充) Approval Manufacturing (CMC)
2002/03/18 SUPPL-1(补充) Approval Manufacturing (CMC)
1998/11/20 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
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 POTASSIUM 剂型/给药途径:TABLET;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
075219 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 1998/08/06 TEVA
075229 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 1998/11/20 RUBICON
075463 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No Yes AB 1999/07/26 RK PHARMA
076561 001 ANDA CATAFLAM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2004/03/18 AMICI PHARMA
215585 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2021/10/08 NOVAST LABS
215750 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2022/05/11 UMEDICA
215787 001 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 50MG Prescription No No AB 2023/03/15 SENORES PHARMS
活性成分:DICLOFENAC POTASSIUM 剂型/给药途径:TABLET;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
076561 002 ANDA CATAFLAM DICLOFENAC POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2021/07/21 AMICI PHARMA
075229 002 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2021/09/16 RUBICON
215787 002 ANDA DICLOFENAC POTASSIUM DICLOFENAC POTASSIUM TABLET;ORAL 25MG Prescription No No AB 2023/11/09 SENORES PHARMS
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database