药品注册申请号:020699
申请类型:NDA (新药申请)
申请人:UPJOHN
申请人全名:UPJOHN US 2 LLC
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 EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Yes No AB 1997/10/20 1997/10/20 Prescription
002 EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Yes No AB 1997/10/20 Prescription
003 EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 100MG BASE No No None 1997/10/20 Discontinued
004 EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Yes Yes AB 1997/10/20 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
2023/08/18 SUPPL-118(补充) Approval Labeling STANDARD
2022/08/15 SUPPL-112(补充) Approval Labeling STANDARD
2021/11/10 SUPPL-113(补充) Approval Labeling STANDARD
2021/09/20 SUPPL-114(补充) Approval Labeling 901 REQUIRED
2017/12/19 SUPPL-111(补充) Approval Labeling 901 REQUIRED
2017/12/19 SUPPL-110(补充) Approval Labeling STANDARD
2017/03/29 SUPPL-108(补充) Approval Labeling STANDARD
2017/01/04 SUPPL-107(补充) Approval Labeling 901 ORDER
2016/02/29 SUPPL-106(补充) Approval Labeling STANDARD
2014/12/17 SUPPL-91(补充) Approval Labeling STANDARD
2014/10/21 SUPPL-104(补充) Approval Labeling STANDARD
2014/07/07 SUPPL-105(补充) Approval Labeling 901 REQUIRED
2014/07/07 SUPPL-103(补充) Approval Labeling STANDARD
2012/12/18 SUPPL-102(补充) Approval Labeling STANDARD
2012/12/18 SUPPL-99(补充) Approval Labeling UNKNOWN
2012/08/24 SUPPL-89(补充) Approval Labeling STANDARD
2012/08/24 SUPPL-49(补充) Approval Labeling STANDARD
2012/05/03 SUPPL-100(补充) Approval Labeling STANDARD
2010/01/06 SUPPL-90(补充) Approval Labeling STANDARD
2009/11/09 SUPPL-86(补充) Approval Labeling STANDARD
2009/01/30 SUPPL-87(补充) Approval Labeling STANDARD
2008/05/23 SUPPL-81(补充) Approval Labeling STANDARD
2008/02/11 SUPPL-83(补充) Approval Labeling STANDARD
2008/02/07 SUPPL-80(补充) Approval Labeling STANDARD
2008/01/30 SUPPL-67(补充) Approval Labeling STANDARD
2007/12/14 SUPPL-47(补充) Approval Efficacy UNKNOWN
2007/09/20 SUPPL-79(补充) Approval Labeling STANDARD
2007/09/20 SUPPL-77(补充) Approval Labeling STANDARD
2007/08/01 SUPPL-75(补充) Approval Labeling STANDARD
2007/08/01 SUPPL-55(补充) Approval Labeling STANDARD
2007/02/07 SUPPL-69(补充) Approval Labeling STANDARD
2006/10/20 SUPPL-72(补充) Approval Labeling STANDARD
2006/09/14 SUPPL-71(补充) Approval Labeling STANDARD
2006/03/02 SUPPL-66(补充) Approval Manufacturing (CMC) N/A
2006/02/24 SUPPL-56(补充) Approval Labeling STANDARD
2006/01/12 SUPPL-64(补充) Approval Labeling STANDARD
2006/01/12 SUPPL-62(补充) Approval Labeling STANDARD
2005/12/01 SUPPL-59(补充) Approval Efficacy STANDARD
2005/11/18 SUPPL-57(补充) Approval Efficacy STANDARD
2005/11/18 SUPPL-54(补充) Approval Efficacy STANDARD
2005/02/18 SUPPL-58(补充) Approval Labeling STANDARD
2004/05/13 SUPPL-52(补充) Approval Labeling STANDARD
2004/05/13 SUPPL-48(补充) Approval Labeling STANDARD
2004/05/13 SUPPL-41(补充) Approval Labeling STANDARD
2004/05/05 SUPPL-30(补充) Approval Efficacy PRIORITY
2004/04/08 SUPPL-46(补充) Approval Labeling STANDARD
2004/03/19 SUPPL-50(补充) Approval Labeling STANDARD
2004/03/19 SUPPL-39(补充) Approval Labeling STANDARD
2004/03/16 SUPPL-45(补充) Approval Labeling STANDARD
2003/09/02 SUPPL-43(补充) Approval Labeling STANDARD
2003/09/02 SUPPL-38(补充) Approval Labeling STANDARD
2003/02/26 SUPPL-32(补充) Approval Labeling STANDARD
2003/02/11 SUPPL-22(补充) Approval Efficacy STANDARD
2003/01/31 SUPPL-34(补充) Approval Labeling STANDARD
2003/01/31 SUPPL-27(补充) Approval Supplement STANDARD
2003/01/31 SUPPL-26(补充) Approval Supplement STANDARD
2003/01/31 SUPPL-23(补充) Approval Supplement STANDARD
2003/01/31 SUPPL-21(补充) Approval Supplement STANDARD
2003/01/31 SUPPL-18(补充) Approval Supplement STANDARD
2003/01/31 SUPPL-14(补充) Approval Supplement STANDARD
2002/11/19 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
2002/10/22 SUPPL-29(补充) Approval Labeling STANDARD
2002/08/07 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2001/10/23 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
2001/08/22 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
2001/05/02 SUPPL-16(补充) Approval Efficacy STANDARD
2001/05/02 SUPPL-15(补充) Approval Efficacy STANDARD
2000/12/13 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
2000/10/31 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
2000/07/20 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
2000/07/13 SUPPL-7(补充) Approval Efficacy STANDARD
2000/06/12 SUPPL-12(补充) Approval Labeling STANDARD
2000/03/09 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
2000/03/09 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
2000/03/03 SUPPL-8(补充) Approval Labeling STANDARD
2000/02/25 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1999/12/21 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1999/03/11 SUPPL-1(补充) Approval Efficacy STANDARD
1998/05/08 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1997/10/20 ORIG-1(原始申请) Approval Type 3 - New Dosage Form STANDARD
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
001 4535186 2007/12/13 PDF格式**本条是由Drugfuture回溯的历史信息**
4535186*PED 2008/06/13 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171 2017/03/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171*PED 2017/09/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6310101 2013/06/28 U-46 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120 2017/03/20 U-535 U-451 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120*PED 2017/09/20 U-451 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958 2017/03/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958*PED 2017/09/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
002 4535186 2007/12/13 PDF格式**本条是由Drugfuture回溯的历史信息**
4535186*PED 2008/06/13 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171 2017/03/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171*PED 2017/09/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6310101 2013/06/28 U-46 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120 2017/03/20 U-451 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120*PED 2017/09/20 U-535 U-451 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958 2017/03/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958*PED 2017/09/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
003 4535186 2007/12/13 PDF格式**本条是由Drugfuture回溯的历史信息**
4535186*PED 2008/06/13 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171 2017/03/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171*PED 2017/09/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120 2017/03/20 U-451 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120*PED 2017/09/20 U-535 U-451 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958 2017/03/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958*PED 2017/09/20 U-459 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
004 4535186 2007/12/13 PDF格式**本条是由Drugfuture回溯的历史信息**
4535186*PED 2008/06/13 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
5916923*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171 2017/03/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6274171*PED 2017/09/20 PDF格式**本条是由Drugfuture回溯的历史信息**
6310101 2013/06/28 U-46 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120 2017/03/20 U-535 U-451 PDF格式**本条是由Drugfuture回溯的历史信息**
6403120*PED 2017/09/20 U-451 U-535 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958 2017/03/20 U-535 U-459 PDF格式**本条是由Drugfuture回溯的历史信息**
6419958*PED 2017/09/20 U-535 U-459 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708 2013/06/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
6444708*PED 2013/12/28 U-398 PDF格式**本条是由Drugfuture回溯的历史信息**
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
001 I-537 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-538 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-561 2010/12/14**本条是由Drugfuture回溯的历史信息**
002 I-537 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-538 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-561 2010/12/14**本条是由Drugfuture回溯的历史信息**
003 I-537 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-538 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-561 2010/12/14**本条是由Drugfuture回溯的历史信息**
004 I-537 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-538 2008/11/18**本条是由Drugfuture回溯的历史信息**
I-561 2010/12/14**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
活性成分:VENLAFAXINE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:EQ 37.5MG 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
020699 001 NDA EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription Yes No AB 1997/10/20 UPJOHN
076565 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2010/06/28 TEVA
078865 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/04/14 WOCKHARDT BIO AG
090174 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/04/14 ZYDUS PHARMS USA INC
200834 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/04/14 AUROBINDO PHARMA LTD
090071 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/04/15 VALEANT PHARMS NORTH
078421 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/05/06 DR REDDYS LABS LTD
090899 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Discontinued No No AB 2011/06/01 TORRENT
091123 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2011/07/11 ORBION PHARMS
204889 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2017/10/05 MACLEODS PHARMS LTD
201272 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2018/11/23 INTELLIPHARMACEUTICS
212277 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2019/07/08 ANNORA PHARMA
203332 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2020/03/12 INVENTIA HLTHCARE
214654 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2021/08/06 YICHANG HUMANWELL
200430 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2023/04/04 NOSTRUM PHARMS LLC
217390 001 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE Prescription No No AB 2023/05/18 GRANULES
活性成分:VENLAFAXINE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:EQ 75MG 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
020699 002 NDA EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription Yes No AB 1997/10/20 UPJOHN
076565 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2010/06/28 TEVA
078865 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/04/14 WOCKHARDT BIO AG
090174 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/04/14 ZYDUS PHARMS USA INC
200834 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/04/14 AUROBINDO PHARMA LTD
090071 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/04/15 VALEANT PHARMS NORTH
078421 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/05/06 DR REDDYS LABS LTD
090899 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Discontinued No No AB 2011/06/01 TORRENT
091123 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2011/07/11 ORBION PHARMS
204889 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2017/10/05 MACLEODS PHARMS LTD
201272 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2018/11/23 INTELLIPHARMACEUTICS
212277 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2019/07/08 ANNORA PHARMA
203332 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2020/03/12 INVENTIA HLTHCARE
214654 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2021/08/06 YICHANG HUMANWELL
200430 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2023/04/04 NOSTRUM PHARMS LLC
217390 002 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE Prescription No No AB 2023/05/18 GRANULES
活性成分:VENLAFAXINE HYDROCHLORIDE 剂型/给药途径:CAPSULE, EXTENDED RELEASE;ORAL 规格:EQ 150MG 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
020699 004 NDA EFFEXOR XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription Yes Yes AB 1997/10/20 UPJOHN
076565 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2010/06/28 TEVA
078865 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/04/14 WOCKHARDT BIO AG
090174 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/04/14 ZYDUS PHARMS USA INC
200834 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/04/14 AUROBINDO PHARMA LTD
090071 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/04/15 VALEANT PHARMS NORTH
078421 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/05/06 DR REDDYS LABS LTD
090899 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Discontinued No No AB 2011/06/01 TORRENT
091123 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2011/07/11 ORBION PHARMS
204889 003 ANDA VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE Prescription No No AB 2017/10/05 MACLEODS PHARMS LTD
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