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 |
| 1986/07/10 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
>>>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 |
| 2025/04/01 |
SUPPL-57(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/05/17 |
SUPPL-53(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/05/17 |
SUPPL-51(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/05/15 |
SUPPL-50(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/05/15 |
SUPPL-49(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/05/15 |
SUPPL-47(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/05/15 |
SUPPL-46(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2015/09/10 |
SUPPL-42(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2013/07/24 |
SUPPL-40(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2011/11/30 |
SUPPL-37(补充) |
Approval |
Labeling-Package Insert |
|
|
|
| 2008/05/29 |
SUPPL-33(补充) |
Approval |
Labeling |
|
|
|
| 2006/09/28 |
SUPPL-31(补充) |
Approval |
Labeling |
|
|
|
| 2006/03/08 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
| 2005/07/06 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
| 2003/04/01 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
| 2002/02/26 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
| 2001/04/12 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC)-Control |
|
|
|
| 2000/05/16 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC)-Facility |
|
|
|
| 2000/05/16 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC)-Facility |
|
|
|
| 1999/07/20 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1999/07/20 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1997/12/05 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1997/04/21 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1997/02/24 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1994/01/12 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1993/07/06 |
SUPPL-6(补充) |
Approval |
Labeling |
|
|
|
| 1993/03/26 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
| 1993/01/12 |
SUPPL-4(补充) |
Approval |
Labeling |
|
|
|
| 1992/03/16 |
SUPPL-3(补充) |
Approval |
Labeling |
|
|
|
| 1989/05/01 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
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 |
| 无 |
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 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
| 050007 |
002 |
NDA |
VIBRAMYCIN |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 100MG BASE |
Discontinued |
Yes |
No |
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 |
| 062337 |
002 |
ANDA |
DOXYCYCLINE HYCLATE |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 100MG BASE |
Prescription |
No |
No |
AB |
1982/03/29
|
STRIDES PHARMA |
| 062396 |
001 |
ANDA |
DOXYCYCLINE HYCLATE |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 100MG BASE |
Prescription |
No |
Yes |
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 |
| 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 LIFESCIENCES |
| 210527 |
002 |
ANDA |
DOXYCYCLINE HYCLATE |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 100MG BASE |
Prescription |
No |
No |
AB |
2018/06/13
|
ALEMBIC |
| 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 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
| 062337 |
001 |
ANDA |
DOXYCYCLINE HYCLATE |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 50MG BASE |
Prescription |
No |
No |
AB |
1982/03/29
|
STRIDES PHARMA |
| 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 |
| 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 LIFESCIENCES |
| 210527 |
001 |
ANDA |
DOXYCYCLINE HYCLATE |
DOXYCYCLINE HYCLATE |
CAPSULE;ORAL |
EQ 50MG BASE |
Prescription |
No |
No |
AB |
2018/06/13
|
ALEMBIC |