美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PAROXETINE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
PAROXETINE HYDROCHLORIDE 204134 002 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 25MG BASE No No 2017/01/20 2017/01/20 LUPIN LTD Prescription
PAROXETINE HYDROCHLORIDE 204134 003 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2017/01/20 2017/01/20 LUPIN LTD Prescription
PAROXETINE MESYLATE 207139 001 ANDA PAROXETINE MESYLATE CAPSULE;ORAL EQ 7.5MG BASE No No 2017/06/20 2017/06/20 ACTAVIS LABS FL INC Prescription
PAROXETINE MESYLATE 207188 001 ANDA PAROXETINE MESYLATE CAPSULE;ORAL EQ 7.5MG BASE No No 2017/08/18 2017/08/18 PRINSTON INC Prescription
PAROXETINE HYDROCHLORIDE 209293 001 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 12.5MG BASE No No 2018/06/12 2018/06/12 SCIECURE PHARMA INC Prescription
PAROXETINE HYDROCHLORIDE 209293 002 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 25MG BASE No No 2018/06/12 2018/06/12 SCIECURE PHARMA INC Prescription
PAROXETINE HYDROCHLORIDE 209293 003 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2018/06/12 2018/06/12 SCIECURE PHARMA INC Prescription
PAROXETINE HYDROCHLORIDE 213485 001 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 12.5MG BASE No No 2021/02/16 2021/02/16 CSPC OUYI Prescription
PAROXETINE HYDROCHLORIDE 213485 002 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 25MG BASE No No 2021/02/16 2021/02/16 CSPC OUYI Prescription
PAROXETINE HYDROCHLORIDE 213485 003 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2021/02/16 2021/02/16 CSPC OUYI Prescription
PAROXETINE HYDROCHLORIDE 213612 001 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 12.5MG BASE No No 2021/08/11 2021/08/11 EPIC PHARMA LLC Discontinued
PAROXETINE HYDROCHLORIDE 213612 002 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 25MG BASE No No 2021/08/11 2021/08/11 EPIC PHARMA LLC Discontinued
PAROXETINE HYDROCHLORIDE 213612 003 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2021/08/11 2022/05/26 EPIC PHARMA LLC Discontinued
PAROXETINE HYDROCHLORIDE 212645 001 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 12.5MG BASE No No 2021/08/27 2021/08/27 CADILA PHARMS LTD Prescription
PAROXETINE HYDROCHLORIDE 212645 002 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 25MG BASE No No 2021/08/27 2021/08/27 CADILA PHARMS LTD Prescription
PAROXETINE HYDROCHLORIDE 212645 003 ANDA PAROXETINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 2021/08/27 2021/08/27 CADILA PHARMS LTD Prescription
PAROXETINE HYDROCHLORIDE 215003 001 ANDA PAROXETINE HYDROCHLORIDE SUSPENSION;ORAL EQ 10MG BASE/5ML No No 2021/09/03 2021/09/03 NOVITIUM PHARMA Prescription
PAROXETINE HYDROCHLORIDE 211248 001 ANDA PAROXETINE HYDROCHLORIDE TABLET;ORAL EQ 10MG BASE No No 2021/11/02 2021/11/02 YILING Prescription
PAROXETINE HYDROCHLORIDE 211248 002 ANDA PAROXETINE HYDROCHLORIDE TABLET;ORAL EQ 20MG BASE No No 2021/11/02 2021/11/02 YILING Prescription
PAROXETINE HYDROCHLORIDE 211248 003 ANDA PAROXETINE HYDROCHLORIDE TABLET;ORAL EQ 30MG BASE No No 2021/11/02 2021/11/02 YILING Prescription
药品名称,活性成分,申请号搜索 高级检索
©2006-2024 DrugFuture->U.S. FDA Drugs Database