药品注册申请号:204621
申请类型:ANDA (仿制药申请)
申请人:ALVOGEN
申请人全名:ALVOGEN 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 NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG No No AB;AB 2015/09/11 2015/07/10 Discontinued
002 NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG No No AB;AB 2015/11/09 Discontinued
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
2022/12/13 SUPPL-6(补充) Approval Labeling STANDARD
2019/08/14 SUPPL-5(补充) Approval Labeling STANDARD
2019/08/14 SUPPL-4(补充) Approval Labeling STANDARD
2015/09/11 ORIG-2(原始申请) Approval
2015/07/10 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:NEVIRAPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:400MG 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
201152 001 NDA VIRAMUNE XR NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued Yes No AB 2011/03/25 BOEHRINGER INGELHEIM
203411 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2014/04/03 SANDOZ
205651 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2014/10/27 MYLAN
204621 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued No No AB 2015/07/10 ALVOGEN
207698 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued No No AB 2017/02/28 AUROBINDO PHARMA
206879 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No Yes AB 2017/10/06 MACLEODS PHARMS LTD
活性成分:NEVIRAPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:400MG 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
201152 001 NDA VIRAMUNE XR NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued Yes No AB 2011/03/25 BOEHRINGER INGELHEIM
203411 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2014/04/03 SANDOZ
205651 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No No AB 2014/10/27 MYLAN
204621 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued No No AB 2015/07/10 ALVOGEN
207698 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Discontinued No No AB 2017/02/28 AUROBINDO PHARMA
206879 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 400MG Prescription No Yes AB 2017/10/06 MACLEODS PHARMS LTD
活性成分:NEVIRAPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:100MG 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
201152 002 NDA VIRAMUNE XR NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued Yes No AB 2012/11/08 BOEHRINGER INGELHEIM
204621 002 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB 2015/11/09 ALVOGEN
208616 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB 2016/11/23 AUROBINDO PHARMA
活性成分:NEVIRAPINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:100MG 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
201152 002 NDA VIRAMUNE XR NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued Yes No AB 2012/11/08 BOEHRINGER INGELHEIM
204621 002 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB 2015/11/09 ALVOGEN
208616 001 ANDA NEVIRAPINE NEVIRAPINE TABLET, EXTENDED RELEASE;ORAL 100MG Discontinued No No AB 2016/11/23 AUROBINDO PHARMA
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