药品注册申请号:076868
申请类型:ANDA (仿制药申请)
申请人:ELITE LABS INC
申请人全名:ELITE LABORATORIES 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 LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 5MG BASE No No AB 2005/08/04 2005/08/04 Prescription
002 LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 10MG BASE No No AB 2005/08/04 Prescription
003 LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 25MG BASE No No AB 2005/08/04 Prescription
004 LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 50MG BASE No No AB 2005/08/04 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
2017/02/23 SUPPL-9(补充) Approval Labeling STANDARD
2015/04/29 SUPPL-8(补充) Approval Labeling
2008/11/19 SUPPL-7(补充) Approval Labeling
2008/09/08 SUPPL-6(补充) Approval Labeling
2005/08/04 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:LOXAPINE SUCCINATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 5MG BASE 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
072204 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 5MG BASE Prescription No No AB 1988/06/15 WATSON LABS
076868 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 5MG BASE Prescription No No AB 2005/08/04 ELITE LABS INC
090695 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 5MG BASE Prescription No No AB 2011/09/26 LANNETT CO INC
活性成分:LOXAPINE SUCCINATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 10MG BASE 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
072205 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 10MG BASE Prescription No No AB 1988/06/15 WATSON LABS
076868 002 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 10MG BASE Prescription No No AB 2005/08/04 ELITE LABS INC
090695 002 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 10MG BASE Prescription No No AB 2011/09/26 LANNETT CO INC
活性成分:LOXAPINE SUCCINATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 25MG BASE 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
072206 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 25MG BASE Prescription No Yes AB 1988/06/15 WATSON LABS
076868 003 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 25MG BASE Prescription No No AB 2005/08/04 ELITE LABS INC
090695 003 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 25MG BASE Prescription No No AB 2011/09/26 LANNETT CO INC
活性成分:LOXAPINE SUCCINATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 50MG BASE 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
072062 001 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 1988/06/15 WATSON LABS
076868 004 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 2005/08/04 ELITE LABS INC
090695 004 ANDA LOXAPINE SUCCINATE LOXAPINE SUCCINATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 2011/09/26 LANNETT CO INC
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