药品注册申请号：021427
申请类型：NDA (新药申请)
申请人：LILLY
申请人全名：ELI LILLY AND CO
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 CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Yes No AB 2004/08/03 2004/08/03 Discontinued
002 CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Yes No AB 2004/08/03 Discontinued
004 CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Yes No AB 2004/08/03 Discontinued
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
>>>原始批准或临时批准<<<
审批日期提交号审批结论提交分类审评优先级；罕用药状态通知信、审评文件、说明书、包装标签备注
2004/08/03 ORIG-1（原始申请） Approval Type 1 - New Molecular Entity STANDARD
>>>补充申请<<<
审批日期提交号审批结论补充类别或审批类型审评优先级；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-57（补充） Approval Labeling-Medication Guide,Labeling-Patient Package Insert STANDARD
2023/08/18 SUPPL-55（补充） Approval Labeling-Package Insert STANDARD
2021/09/20 SUPPL-56（补充） Approval Labeling-Package Insert 901 REQUIRED
2020/10/01 SUPPL-53（补充） Approval Labeling-Package Insert STANDARD
2020/04/20 SUPPL-52（补充） Approval Efficacy-New Patient Population STANDARD
2019/10/04 SUPPL-51（补充） Approval Labeling-Package Insert STANDARD
2017/12/19 SUPPL-50（补充） Approval Labeling-Package Insert 901 REQUIRED
2017/01/04 SUPPL-49（补充） Approval Labeling-Package Insert 901 REQUIRED
2016/09/02 SUPPL-48（补充） Approval Labeling-Package Insert 901 REQUIRED
2016/07/12 SUPPL-47（补充） Approval Manufacturing (CMC) STANDARD
2015/06/18 SUPPL-46（补充） Approval Labeling-Package Insert STANDARD
2014/11/25 SUPPL-42（补充） Approval Labeling-Package Insert STANDARD
2014/11/25 SUPPL-37（补充） Approval Labeling-Package Insert STANDARD
2014/10/16 SUPPL-44（补充） Approval Efficacy-New Patient Population STANDARD
2014/10/16 SUPPL-43（补充） Approval Efficacy-Pediatric STANDARD
2014/07/17 SUPPL-45（补充） Approval Labeling-Package Insert 901 REQUIRED
2012/10/18 SUPPL-41（补充） Approval Efficacy-New Patient Population PRIORITY
2012/10/18 SUPPL-40（补充） Approval Labeling-Package Insert,Labeling-Medication Guide STANDARD
2012/08/24 SUPPL-38（补充） Approval Labeling STANDARD
2012/08/24 SUPPL-32（补充） Approval Labeling-Medication Guide STANDARD
2011/09/02 SUPPL-39（补充） Approval Labeling-Package Insert 901 REQUIRED
2011/04/12 SUPPL-36（补充） Approval Labeling STANDARD
2011/03/04 SUPPL-31（补充） Approval Labeling STANDARD
2009/11/19 SUPPL-30（补充） Approval Efficacy-New Indication STANDARD
2009/03/18 SUPPL-28（补充） Approval Labeling STANDARD
2009/03/18 SUPPL-27（补充） Approval Labeling STANDARD
2009/03/18 SUPPL-21（补充） Approval Labeling STANDARD
2009/01/30 SUPPL-29（补充） Approval Labeling 901 REQUIRED
2007/11/28 SUPPL-17（补充） Approval Labeling STANDARD
2007/11/28 SUPPL-15（补充） Approval Efficacy-New Indication UNKNOWN
2007/08/02 SUPPL-18（补充） Approval Labeling STANDARD
2007/02/23 SUPPL-13（补充） Approval Labeling STANDARD
2007/02/23 SUPPL-11（补充） Approval Efficacy-New Indication UNKNOWN
2007/02/23 SUPPL-9（补充） Approval Labeling STANDARD
2006/09/20 SUPPL-12（补充） Approval Labeling STANDARD
2006/06/06 SUPPL-7（补充） Approval Labeling STANDARD
2005/02/18 SUPPL-2（补充） Approval Labeling 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 5023269 2013/06/11 Y Y U-795 U-796 U-799 U-398 U-882 U-605 U-797 U-839 PDF格式**本条是由Drugfuture回溯的历史信息**
5023269*PED 2013/12/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5508276 2014/07/18 Y PDF格式**本条是由Drugfuture回溯的历史信息**
5508276*PED 2015/01/18 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756 2019/09/10 U-882 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756*PED 2020/03/10 PDF格式**本条是由Drugfuture回溯的历史信息**
002 5023269 2013/06/11 Y Y U-797 U-839 U-605 U-795 U-796 U-799 U-398 U-882 PDF格式**本条是由Drugfuture回溯的历史信息**
5023269*PED 2013/12/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5508276 2014/07/18 Y PDF格式**本条是由Drugfuture回溯的历史信息**
5508276*PED 2015/01/18 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756 2019/09/10 U-882 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756*PED 2020/03/10 PDF格式**本条是由Drugfuture回溯的历史信息**
004 5023269 2013/06/11 Y Y U-398 U-882 U-795 U-796 U-799 U-605 U-797 U-839 PDF格式**本条是由Drugfuture回溯的历史信息**
5023269*PED 2013/12/11 PDF格式**本条是由Drugfuture回溯的历史信息**
5508276 2014/07/18 Y PDF格式**本条是由Drugfuture回溯的历史信息**
5508276*PED 2015/01/18 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756 2019/09/10 U-882 PDF格式**本条是由Drugfuture回溯的历史信息**
6596756*PED 2020/03/10 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-470 2007/09/03**本条是由Drugfuture回溯的历史信息**
I-524 2010/02/23**本条是由Drugfuture回溯的历史信息**
I-566 2011/06/13**本条是由Drugfuture回溯的历史信息**
I-632 2013/11/04**本条是由Drugfuture回溯的历史信息**
M-61 2015/10/18**本条是由Drugfuture回溯的历史信息**
M-71 2010/11/28**本条是由Drugfuture回溯的历史信息**
NCE 2009/08/03**本条是由Drugfuture回溯的历史信息**
NPP 2017/10/16**本条是由Drugfuture回溯的历史信息**
NPP 2023/04/20**本条是由Drugfuture回溯的历史信息**
PED 2014/05/04**本条是由Drugfuture回溯的历史信息**
PED 2016/04/18**本条是由Drugfuture回溯的历史信息**
002 I-470 2007/09/03**本条是由Drugfuture回溯的历史信息**
I-524 2010/02/23**本条是由Drugfuture回溯的历史信息**
I-566 2011/06/13**本条是由Drugfuture回溯的历史信息**
I-632 2013/11/04**本条是由Drugfuture回溯的历史信息**
M-61 2015/10/18**本条是由Drugfuture回溯的历史信息**
M-71 2010/11/28**本条是由Drugfuture回溯的历史信息**
NCE 2009/08/03**本条是由Drugfuture回溯的历史信息**
NPP 2017/10/16**本条是由Drugfuture回溯的历史信息**
NPP 2023/04/20**本条是由Drugfuture回溯的历史信息**
PED 2014/05/04**本条是由Drugfuture回溯的历史信息**
PED 2016/04/18**本条是由Drugfuture回溯的历史信息**
004 I-470 2007/09/03**本条是由Drugfuture回溯的历史信息**
I-524 2010/02/23**本条是由Drugfuture回溯的历史信息**
I-566 2011/06/13**本条是由Drugfuture回溯的历史信息**
I-632 2013/11/04**本条是由Drugfuture回溯的历史信息**
M-61 2015/10/18**本条是由Drugfuture回溯的历史信息**
M-71 2010/11/28**本条是由Drugfuture回溯的历史信息**
NCE 2009/08/03**本条是由Drugfuture回溯的历史信息**
NPP 2017/10/16**本条是由Drugfuture回溯的历史信息**
NPP 2023/04/20**本条是由Drugfuture回溯的历史信息**
PED 2014/05/04**本条是由Drugfuture回溯的历史信息**
PED 2016/04/18**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:DULOXETINE HYDROCHLORIDE; 剂型/给药途径:CAPSULE, DELAYED REL PELLETS;ORAL; 规格:EQ 20MG 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
021427 001 NDA CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued Yes No AB 2004/08/03 LILLY
090694 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2013/12/11 LUPIN LTD
090723 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued No No AB 2013/12/11 GRAVITI PHARMS
090745 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued No No AB 2013/12/11 SUN PHARM
090774 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued No No AB 2013/12/11 TORRENT
090778 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2013/12/11 AUROBINDO PHARMA LTD
090776 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2013/12/17 ACTAVIS ELIZABETH
090728 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2014/01/08 ZYDUS PHARMS
090739 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2014/01/08 ZYDUS HLTHCARE
202949 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2014/06/09 ALEMBIC
203088 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2014/06/11 BRECKENRIDGE
202045 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued No No AB 2014/06/11 APOTEX
203197 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2015/08/26 ALKEM LABS LTD
202336 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2015/10/28 INVENTIA
090780 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Discontinued No No AB 2015/10/28 PH HEALTH
204343 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2016/08/03 HETERO LABS LTD III
208706 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2017/01/06 AJANTA PHARMA LTD
204815 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2017/03/23 MACLEODS PHARMS LTD
206653 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2017/05/18 PRINSTON INC
211310 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2018/10/16 CSPC OUYI
210599 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2019/04/17 QINGDAO BAHEAL PHARM
212328 001 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 20MG BASE Prescription No No AB 2021/02/11 SUNSHINE
>>>活性成分:DULOXETINE HYDROCHLORIDE; 剂型/给药途径:CAPSULE, DELAYED REL PELLETS;ORAL; 规格:EQ 30MG 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
021427 002 NDA CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued Yes No AB 2004/08/03 LILLY
090694 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2013/12/11 LUPIN LTD
090723 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued No No AB 2013/12/11 GRAVITI PHARMS
090745 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued No No AB 2013/12/11 SUN PHARM
090774 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued No No AB 2013/12/11 TORRENT
090778 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2013/12/11 AUROBINDO PHARMA LTD
090776 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2013/12/17 ACTAVIS ELIZABETH
090728 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2014/01/08 ZYDUS PHARMS
090739 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2014/01/08 ZYDUS HLTHCARE
202949 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2014/06/09 ALEMBIC
203088 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2014/06/11 BRECKENRIDGE
202045 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued No No AB 2014/06/11 APOTEX
203197 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2015/08/26 ALKEM LABS LTD
202336 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2015/10/28 INVENTIA
090780 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Discontinued No No AB 2015/10/28 PH HEALTH
204343 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2016/08/03 HETERO LABS LTD III
208706 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2017/01/06 AJANTA PHARMA LTD
204815 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2017/03/23 MACLEODS PHARMS LTD
206653 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2017/05/18 PRINSTON INC
211310 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2018/10/16 CSPC OUYI
210599 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2019/04/17 QINGDAO BAHEAL PHARM
212328 002 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 30MG BASE Prescription No No AB 2021/02/11 SUNSHINE
>>>活性成分:DULOXETINE HYDROCHLORIDE; 剂型/给药途径:CAPSULE, DELAYED REL PELLETS;ORAL; 规格:EQ 60MG 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
021427 004 NDA CYMBALTA DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued Yes No AB 2004/08/03 LILLY
090694 004 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2013/12/11 LUPIN LTD
090723 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued No No AB 2013/12/11 GRAVITI PHARMS
090745 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued No No AB 2013/12/11 SUN PHARM
090774 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued No No AB 2013/12/11 TORRENT
090778 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2013/12/11 AUROBINDO PHARMA LTD
090776 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2013/12/17 ACTAVIS ELIZABETH
090728 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2014/01/08 ZYDUS PHARMS
090739 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2014/01/08 ZYDUS HLTHCARE
202949 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2014/06/09 ALEMBIC
203088 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2014/06/11 BRECKENRIDGE
202045 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued No No AB 2014/06/11 APOTEX
203197 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2015/08/26 ALKEM LABS LTD
202336 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2015/10/28 INVENTIA
090780 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Discontinued No No AB 2015/10/28 PH HEALTH
204343 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2016/08/03 HETERO LABS LTD III
208706 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No Yes AB 2017/01/06 AJANTA PHARMA LTD
204815 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2017/03/23 MACLEODS PHARMS LTD
206653 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2017/05/18 PRINSTON INC
211310 003 ANDA DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED REL PELLETS;ORAL EQ 60MG BASE Prescription No No AB 2018/10/16 CSPC OUYI
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