药品注册申请号:090025
申请类型:ANDA (仿制药申请)
申请人:LUPIN
申请人全名:LUPIN 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 LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM No No AB 2009/01/15 2009/01/15 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
2024/01/24 SUPPL-44(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-41(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-39(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-34(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-30(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-29(补充) Approval Labeling STANDARD
2024/01/24 SUPPL-28(补充) Approval Labeling STANDARD
2016/01/14 SUPPL-22(补充) Approval Labeling STANDARD
2016/01/14 SUPPL-21(补充) Approval Labeling STANDARD
2016/01/14 SUPPL-20(补充) Approval Labeling STANDARD
2014/09/26 SUPPL-19(补充) Approval Labeling STANDARD
2014/09/26 SUPPL-15(补充) Approval Labeling STANDARD
2012/07/19 SUPPL-11(补充) Approval REMS
2011/09/20 SUPPL-9(补充) Approval Labeling
2009/11/16 SUPPL-6(补充) Approval Labeling
2009/01/15 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:LEVETIRACETAM 剂型/给药途径:TABLET;ORAL 规格:1GM 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
021035 004 NDA KEPPRA LEVETIRACETAM TABLET;ORAL 1GM Prescription Yes Yes AB 2006/01/06 UCB INC
078042 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 STRIDES PHARMA
078858 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 TORRENT PHARMS
078993 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 AUROBINDO PHARMA
079042 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 INGENUS PHARMS LLC
090025 001 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 LUPIN
078904 001 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/01/15 DR REDDYS LABS LTD
078106 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/02/10 PRINSTON INC
078869 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/03/13 VIWIT PHARM
078918 002 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/04/29 ZYDUS PHARMS USA INC
090261 001 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2009/12/08 MYLAN
078960 001 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2010/02/01 TARO
090767 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2010/07/28 RISING
090484 001 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2010/08/05 ORBION PHARMS
090515 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2010/10/08 HETERO LABS LTD III
091491 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2010/12/14 ZHEJIANG JINGXIN
090843 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Discontinued No No AB 2011/02/14 ACCORD HLTHCARE
201293 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2011/06/14 CHARTWELL RX
215069 002 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2021/06/11 SCIEGEN PHARMS INC
216375 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2022/05/27 ALKEM LABS LTD
214815 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Prescription No No AB 2022/10/07 MSN
217878 004 ANDA LEVETIRACETAM LEVETIRACETAM TABLET;ORAL 1GM Discontinued No No AB 2023/06/13 GRANULES
更多信息
药品NDC数据与药品包装、标签说明书
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