美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DULOXETINE HYDROCHLORIDE"
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
DULOXETINE HYDROCHLORIDE 090669 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL EQ 20MG BASE No 2010/11/18 (TA) IMPAX LABS INC None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090669 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL EQ 30MG BASE No 2010/11/18 (TA) IMPAX LABS INC None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090669 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL EQ 60MG BASE No 2010/11/18 (TA) IMPAX LABS INC None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090775 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 20MG No 2011/02/02 (TA) SANDOZ None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090775 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 30MG No 2011/02/02 (TA) SANDOZ None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090775 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 60MG No 2011/02/02 (TA) SANDOZ None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090773 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 20MG No 2011/07/06 (TA) WOCKHARDT None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090773 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 30MG No 2011/07/06 (TA) WOCKHARDT None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090773 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE; ORAL 60MG No 2011/07/06 (TA) WOCKHARDT None (Tentative Approval)
DULOXETINE HYDROCHLORIDE 090694 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE No No 2013/12/11 2013/12/11 LUPIN LTD Prescription
DULOXETINE HYDROCHLORIDE 090694 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE No No 2013/12/11 2013/12/11 LUPIN LTD Prescription
DULOXETINE HYDROCHLORIDE 090694 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 40MG BASE No No 2013/12/11 2013/12/11 LUPIN LTD Prescription
DULOXETINE HYDROCHLORIDE 090694 004 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE No No 2013/12/11 2013/12/11 LUPIN LTD Prescription
DULOXETINE HYDROCHLORIDE 090723 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE No No 2013/12/11 2013/12/11 MARKSANS PHARMA Prescription
DULOXETINE HYDROCHLORIDE 090723 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE No No 2013/12/11 2013/12/11 MARKSANS PHARMA Prescription
DULOXETINE HYDROCHLORIDE 090723 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE No No 2013/12/11 2013/12/11 MARKSANS PHARMA Prescription
DULOXETINE HYDROCHLORIDE 090745 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE No No 2013/12/11 2013/12/11 SUN PHARM Prescription
DULOXETINE HYDROCHLORIDE 090745 002 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE No No 2013/12/11 2013/12/11 SUN PHARM Prescription
DULOXETINE HYDROCHLORIDE 090745 003 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE No No 2013/12/11 2013/12/11 SUN PHARM Prescription
DULOXETINE HYDROCHLORIDE 090774 001 ANDA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE No No 2013/12/11 2013/12/11 TORRENT Prescription
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