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 |
| 1982/04/12 |
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 |
| 2016/11/08 |
SUPPL-28(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/03/30 |
SUPPL-27(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/06/03 |
SUPPL-26(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2005/04/04 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
| 2003/06/13 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
| 2002/08/22 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
| 1993/12/27 |
SUPPL-19(补充) |
Approval |
Labeling |
|
|
|
| 1993/09/08 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1991/02/11 |
SUPPL-18(补充) |
Approval |
Labeling |
|
|
|
| 1991/02/11 |
SUPPL-17(补充) |
Approval |
Labeling |
|
|
|
| 1991/02/11 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
| 1990/06/19 |
SUPPL-15(补充) |
Approval |
Labeling |
|
|
|
| 1989/06/20 |
SUPPL-13(补充) |
Approval |
Labeling |
|
|
|
| 1989/02/07 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1988/12/09 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1987/04/07 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1985/10/22 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1984/12/13 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1984/12/13 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 1984/03/16 |
SUPPL-3(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:HYDROXYZINE HYDROCHLORIDE; 剂型/给药途径:SYRUP;ORAL; 规格:10MG/5ML; 治疗等效代码:AA<<<
| 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 |
| 087294 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Prescription |
Yes |
Yes |
AA |
1982/04/12
|
CHARTWELL RX |
| 040010 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Discontinued |
No |
No |
AA |
1994/10/28
|
HIKMA |
| 040391 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Prescription |
No |
No |
AA |
2002/04/10
|
PAI HOLDINGS PHARM |
| 201674 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Prescription |
No |
No |
AA |
2013/08/21
|
LANNETT CO INC |
| 210634 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Prescription |
No |
No |
AA |
2019/02/26
|
APOZEAL PHARMS |
| 219289 |
001 |
ANDA |
HYDROXYZINE HYDROCHLORIDE |
HYDROXYZINE HYDROCHLORIDE |
SYRUP;ORAL |
10MG/5ML |
Prescription |
No |
No |
AA |
2025/04/28
|
BIONPHARMA |