药品注册申请号:062031
申请类型:ANDA (仿制药申请)
申请人:ACTAVIS LABS FL INC
申请人全名:ACTAVIS LABORATORIES FL 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 DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE No No AB 1982/10/13 Approved Prior to Jan 1, 1982 Prescription
002 DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE No No AB 1982/10/13 Prescription
批准历史,通知信,药品说明书,综述等审批信息
批准日期申请类型申请提交号审查批准结论申请内容分类审评分类(优先审评;罕用药状态)通知信、综述、标签、说明书备注
2018/01/02 SUPPL 80 Approval Labeling STANDARD
2018/01/02 SUPPL 79 Approval Labeling STANDARD
2014/04/30 SUPPL 74 Approval Labeling STANDARD
2010/07/28 SUPPL 63 Approval Labeling
2005/09/01 SUPPL 43 Approval Labeling
2002/12/23 SUPPL 39 Approval Labeling
2002/02/20 SUPPL 38 Approval Labeling
2001/04/25 SUPPL 37 Approval Manufacturing (CMC)
2001/02/08 SUPPL 36 Approval Manufacturing (CMC)
2000/08/09 SUPPL 35 Approval Labeling
1999/06/16 SUPPL 34 Approval Manufacturing (CMC)
1998/10/23 SUPPL 32 Approval Manufacturing (CMC)
1998/08/10 SUPPL 31 Approval Manufacturing (CMC)
1998/08/10 SUPPL 30 Approval Manufacturing (CMC)
1998/08/10 SUPPL 29 Approval Manufacturing (CMC)
1993/09/01 SUPPL 28 Approval Labeling
1993/04/14 SUPPL 27 Approval Labeling
1992/10/23 SUPPL 26 Approval Labeling
1992/02/26 SUPPL 25 Approval Labeling
1991/05/31 SUPPL 23 Approval Manufacturing (CMC)
1991/05/31 SUPPL 20 Approval Manufacturing (CMC)
1990/11/15 SUPPL 24 Approval Manufacturing (CMC)
1990/11/15 SUPPL 21 Approval Manufacturing (CMC)
1988/05/16 SUPPL 16 Approval Manufacturing (CMC)
1982/10/13 ORIG 1 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:DOXYCYCLINE HYCLATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 100MG 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
050007 002 NDA VIBRAMYCIN DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription Yes Yes AB Approved Prior to Jan 1, 1982 PFIZER
062031 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB Approved Prior to Jan 1, 1982 ACTAVIS LABS FL INC
062396 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 1984/05/07 HIKMA INTL PHARMS
062500 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 1984/09/11 CHARTWELL LIFE SCI
062676 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 1986/07/10 SUN PHARM INDUSTRIES
207289 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 2016/06/27 AMNEAL PHARMS
207774 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 2018/05/31 ZYDUS PHARMS
210527 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 2018/06/13 ALEMBIC PHARMS LTD
209402 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 100MG BASE Prescription No No AB 2019/10/07 CHANGZHOU PHARM
活性成分:DOXYCYCLINE HYCLATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 50MG 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
062031 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 1982/10/13 ACTAVIS LABS FL INC
062500 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 1984/09/11 CHARTWELL LIFE SCI
062396 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 1984/11/07 HIKMA INTL PHARMS
062676 002 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 1986/07/10 SUN PHARM INDUSTRIES
207774 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 2018/05/31 ZYDUS PHARMS
210527 001 ANDA DOXYCYCLINE HYCLATE DOXYCYCLINE HYCLATE CAPSULE;ORAL EQ 50MG BASE Prescription No No AB 2018/06/13 ALEMBIC PHARMS LTD
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2019 DrugFuture->U.S. FDA Drugs Database