药品注册申请号:206751
申请类型:ANDA (仿制药申请)
申请人:ZYDUS PHARMS
申请人全名:ZYDUS 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 METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG No No AB 2018/04/23 2018/04/23 Prescription
002 METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 8MG No No AB 2018/04/23 Prescription
003 METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 16MG No No AB 2018/04/23 Prescription
004 METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 32MG No No AB 2018/04/23 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
2018/04/23 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:METHYLPREDNISOLONE 剂型/给药途径:TABLET;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
011153 001 NDA MEDROL METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription Yes No AB Approved Prior to Jan 1, 1982 PFIZER
040232 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 1997/10/16 WATSON LABS
040189 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 1997/10/31 JUBILANT CADISTA
040194 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 1997/10/31 SANDOZ
040183 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 1998/12/22 ENDO OPERATIONS
206751 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 2018/04/23 ZYDUS PHARMS
204072 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Prescription No No AB 2018/05/14 TIANJIN TIANYAO
212262 001 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 4MG Discontinued No No AB 2019/06/27 PRAXGEN
活性成分:METHYLPREDNISOLONE 剂型/给药途径:TABLET;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
011153 004 NDA MEDROL METHYLPREDNISOLONE TABLET;ORAL 8MG Prescription Yes No AB Approved Prior to Jan 1, 1982 PFIZER
040189 002 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 8MG Prescription No No AB 1997/10/31 JUBILANT CADISTA
206751 002 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 8MG Prescription No No AB 2018/04/23 ZYDUS PHARMS
活性成分:METHYLPREDNISOLONE 剂型/给药途径:TABLET;ORAL 规格:16MG 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
011153 003 NDA MEDROL METHYLPREDNISOLONE TABLET;ORAL 16MG Prescription Yes No AB Approved Prior to Jan 1, 1982 PFIZER
040189 003 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 16MG Prescription No No AB 2007/07/20 JUBILANT CADISTA
206751 003 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 16MG Prescription No No AB 2018/04/23 ZYDUS PHARMS
活性成分:METHYLPREDNISOLONE 剂型/给药途径:TABLET;ORAL 规格:32MG 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
011153 006 NDA MEDROL METHYLPREDNISOLONE TABLET;ORAL 32MG Prescription Yes Yes AB Approved Prior to Jan 1, 1982 PFIZER
040189 004 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 32MG Prescription No No AB 2007/07/20 JUBILANT CADISTA
206751 004 ANDA METHYLPREDNISOLONE METHYLPREDNISOLONE TABLET;ORAL 32MG Prescription No No AB 2018/04/23 ZYDUS PHARMS
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