药品注册申请号:090120
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 QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE No No AB 2012/03/27 2012/03/27 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
2023/02/08 SUPPL-16(补充) Approval Labeling STANDARD
2023/02/08 SUPPL-13(补充) Approval Labeling STANDARD
2023/02/08 SUPPL-12(补充) Approval Labeling STANDARD
2023/02/08 SUPPL-11(补充) Approval Labeling STANDARD
2019/12/11 SUPPL-9(补充) Approval Labeling STANDARD
2019/12/11 SUPPL-8(补充) Approval Labeling STANDARD
2017/06/30 SUPPL-7(补充) Approval Labeling STANDARD
2017/06/30 SUPPL-6(补充) Approval Labeling STANDARD
2015/08/25 SUPPL-4(补充) Approval Labeling STANDARD
2015/08/25 SUPPL-2(补充) Approval Labeling STANDARD
2012/03/27 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:QUETIAPINE FUMARATE 剂型/给药途径:TABLET;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
020639 001 NDA SEROQUEL QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription Yes Yes AB 1997/09/26 ASTRAZENECA
077380 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 DR REDDYS LABS LTD
077745 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 TEVA PHARMS
090120 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 HIKMA
090960 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 SCIEGEN PHARMS INC
091388 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 AUROBINDO PHARMA LTD
201109 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 LUPIN LTD
201190 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 SUN PHARM
202152 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2012/03/27 ACCORD HLTHCARE
078679 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Discontinued No No AB 2012/12/14 CHARTWELL RX
201504 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2013/02/12 ALKEM LABS LTD
202674 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2016/03/08 UNICHEM
203359 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2016/05/17 MACLEODS PHARMS LTD
204316 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2022/06/16 HETERO LABS LTD V
206954 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2022/08/24 PRINSTON INC
205983 001 ANDA QUETIAPINE FUMARATE QUETIAPINE FUMARATE TABLET;ORAL EQ 25MG BASE Prescription No No AB 2024/05/20 IPCA LABS LTD
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