药品注册申请号:065413
申请类型:ANDA (仿制药申请)
申请人:HIKMA
申请人全名:HIKMA PHARMACEUTICALS USA INC
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 MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG No No AB 2008/07/29 2008/07/29 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
2024/08/13 SUPPL-24(补充) Approval REMS
2024/02/07 SUPPL-23(补充) Approval Labeling STANDARD
2024/02/07 SUPPL-22(补充) Approval Labeling STANDARD
2024/02/07 SUPPL-21(补充) Approval Labeling STANDARD
2021/08/11 SUPPL-20(补充) Approval REMS
2021/05/17 SUPPL-17(补充) Approval Labeling STANDARD
2021/04/21 SUPPL-18(补充) Approval REMS
2021/01/15 SUPPL-15(补充) Approval REMS
2020/06/16 SUPPL-14(补充) Approval Labeling STANDARD
2019/11/27 SUPPL-13(补充) Approval Labeling STANDARD
2015/11/13 SUPPL-10(补充) Approval REMS
2015/10/30 SUPPL-11(补充) Approval Labeling STANDARD
2014/09/12 SUPPL-6(补充) Approval Manufacturing (CMC)
2013/09/27 SUPPL-9(补充) Approval Labeling STANDARD
2012/09/25 SUPPL-8(补充) Approval REMS
2012/07/25 SUPPL-7(补充) Approval Labeling STANDARD
2010/02/02 SUPPL-4(补充) Approval Labeling
2009/09/09 SUPPL-3(补充) Approval Labeling
2009/02/20 SUPPL-2(补充) Approval Labeling
2008/07/29 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:MYCOPHENOLATE MOFETIL 剂型/给药途径:TABLET;ORAL 规格:500MG 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
050723 001 NDA CELLCEPT MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription Yes Yes AB 1997/06/19 ROCHE PALO
065413 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2008/07/29 HIKMA
065451 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2008/10/15 SANDOZ
065521 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2009/05/04 MYLAN
065416 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2009/05/04 ACCORD HLTHCARE
090456 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2010/06/10 STRIDES PHARMA
090606 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Discontinued No No AB 2010/07/16 AMNEAL
091249 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2011/11/04 ALKEM LABS LTD
204076 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2017/11/16 ZHEJIANG HISUN PHARM
212087 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2020/07/31 CONCORD BIOTECH LTD
217937 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2024/02/20 AUROBINDO PHARMA
208119 001 ANDA MYCOPHENOLATE MOFETIL MYCOPHENOLATE MOFETIL TABLET;ORAL 500MG Prescription No No AB 2024/10/22 HETERO LABS LTD V
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