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 |
2021/02/16 |
SUPPL-52(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2021/02/16 |
SUPPL-51(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/01/24 |
SUPPL-48(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2011/07/27 |
SUPPL-44(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2008/06/16 |
SUPPL-43(补充) |
Approval |
Labeling |
|
|
|
2003/01/03 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2002/04/29 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/11/09 |
SUPPL-30(补充) |
Approval |
Labeling |
|
|
|
2001/11/09 |
SUPPL-29(补充) |
Approval |
Labeling |
|
|
|
2000/02/29 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/12/21 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/09/23 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/05/20 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/12/01 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/09/15 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/07/09 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1996/09/20 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
1996/04/10 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
1995/01/12 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
1994/12/23 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1994/10/11 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1992/04/03 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1992/04/03 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1991/08/16 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1991/08/16 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1991/05/09 |
SUPPL-11(补充) |
Approval |
Labeling |
|
|
|
1990/01/04 |
SUPPL-10(补充) |
Approval |
Labeling |
|
|
|
1987/11/18 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/11/18 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/09/25 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/06/15 |
ORIG-1(原始申请) |
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 |
无 |
与本品治疗等效的药品
活性成分:HYDROXYZINE PAMOATE 剂型/给药途径:CAPSULE;ORAL 规格:EQ 25MG HYDROCHLORIDE 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 |
011459 |
002 |
NDA |
VISTARIL |
HYDROXYZINE PAMOATE |
CAPSULE;ORAL |
EQ 25MG HYDROCHLORIDE |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
PFIZER |
087479 |
001 |
ANDA |
HYDROXYZINE PAMOATE |
HYDROXYZINE PAMOATE |
CAPSULE;ORAL |
EQ 25MG HYDROCHLORIDE |
Prescription |
No |
No |
AB |
Approved Prior to Jan 1, 1982
|
SANDOZ |
088496 |
001 |
ANDA |
HYDROXYZINE PAMOATE |
HYDROXYZINE PAMOATE |
CAPSULE;ORAL |
EQ 25MG HYDROCHLORIDE |
Prescription |
No |
No |
AB |
1984/06/15
|
BARR |
040156 |
001 |
ANDA |
HYDROXYZINE PAMOATE |
HYDROXYZINE PAMOATE |
CAPSULE;ORAL |
EQ 25MG HYDROCHLORIDE |
Prescription |
No |
No |
AB |
1996/07/15
|
IMPAX LABS INC |
201507 |
001 |
ANDA |
HYDROXYZINE PAMOATE |
HYDROXYZINE PAMOATE |
CAPSULE;ORAL |
EQ 25MG HYDROCHLORIDE |
Prescription |
No |
No |
AB |
2013/06/03
|
HERITAGE PHARMA |