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 |
2009/03/20 |
SUPPL-45(补充) |
Approval |
Labeling |
|
|
|
2002/10/04 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2002/07/29 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2001/09/12 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/10/26 |
SUPPL-34(补充) |
Approval |
Labeling |
|
|
|
2000/07/25 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
2000/01/28 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/09/24 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/09/24 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/09/24 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1999/08/20 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/12/09 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1998/03/10 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1997/10/17 |
SUPPL-26(补充) |
Approval |
Labeling |
|
|
|
1997/05/30 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1994/10/13 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1989/07/27 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
1987/11/12 |
SUPPL-20(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/11/12 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1987/03/06 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1984/03/08 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1983/11/02 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1982/11/12 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
1980/01/10 |
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:CYPROHEPTADINE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:4MG 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 |
087056 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Discontinued |
Yes |
No |
AA |
Approved Prior to Jan 1, 1982
|
HERITAGE PHARMA |
088212 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
1983/05/26
|
CHARTWELL RX |
040537 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2003/09/30
|
MOUNTAIN |
040644 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2006/05/30
|
KENTON |
205087 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2015/09/23
|
NOVAST LABS |
206553 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2016/11/29
|
APPCO |
207783 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Discontinued |
No |
No |
AA |
2016/12/29
|
RISING |
207555 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2017/01/31
|
RISING |
208938 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
Yes |
AA |
2017/05/19
|
ZYDUS PHARMS |
209172 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2018/04/11
|
STRIDES PHARMA |
206676 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2019/04/12
|
BEXIMCO PHARMS USA |
212491 |
001 |
ANDA |
CYPROHEPTADINE HYDROCHLORIDE |
CYPROHEPTADINE HYDROCHLORIDE |
TABLET;ORAL |
4MG |
Prescription |
No |
No |
AA |
2021/02/24
|
QUAGEN |