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 |
| 1998/08/12 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
STANDARD
|
|
|
>>>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 |
| 2025/06/27 |
SUPPL-52(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2024/08/13 |
SUPPL-51(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2022/08/10 |
SUPPL-48(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2022/06/06 |
SUPPL-49(补充) |
Approval |
Efficacy-New Patient Population |
STANDARD
|
|
|
| 2022/06/06 |
SUPPL-47(补充) |
Approval |
Efficacy-New Patient Population |
STANDARD
|
|
|
| 2021/10/22 |
SUPPL-43(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2021/10/22 |
SUPPL-42(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/08/11 |
SUPPL-45(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2021/04/21 |
SUPPL-44(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2021/01/15 |
SUPPL-41(补充) |
Approval |
REMS - MODIFIED - D-N-A |
N/A
|
|
|
| 2019/12/13 |
SUPPL-37(补充) |
Approval |
Labeling-Container/Carton Labels,Labeling-Package Insert |
STANDARD
|
|
|
| 2019/02/27 |
SUPPL-35(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/08/23 |
SUPPL-33(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2017/12/18 |
SUPPL-34(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/05/26 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2015/11/13 |
SUPPL-31(补充) |
Approval |
REMS-Modified |
N/A
|
|
|
| 2015/07/09 |
SUPPL-30(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2013/09/27 |
SUPPL-29(补充) |
Approval |
REMS-Proposal |
N/A
|
|
|
| 2013/09/27 |
SUPPL-28(补充) |
Approval |
Labeling,Labeling-Package Insert |
STANDARD
|
|
|
| 2013/02/14 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2012/09/25 |
SUPPL-20(补充) |
Approval |
REMS-Proposal,Labeling |
STANDARD
|
|
|
| 2012/06/22 |
SUPPL-26(补充) |
Approval |
Labeling-Medication Guide |
STANDARD
|
|
|
| 2012/06/08 |
SUPPL-24(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2009/10/08 |
SUPPL-22(补充) |
Approval |
Labeling-Medication Guide |
UNKNOWN
|
|
|
| 2009/06/18 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2009/02/27 |
SUPPL-18(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2008/12/15 |
SUPPL-17(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2008/05/09 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2007/12/20 |
SUPPL-13(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2007/09/21 |
SUPPL-14(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2005/10/17 |
SUPPL-12(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2005/04/12 |
SUPPL-10(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2003/02/28 |
SUPPL-5(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2002/12/17 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2002/02/27 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 2000/07/28 |
SUPPL-4(补充) |
Approval |
Efficacy-New Indication |
STANDARD
|
|
|
| 2000/07/27 |
SUPPL-3(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2000/06/16 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 2000/04/20 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
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 |
| 001 |
4753935 |
2009/05/03 |
Y |
Y |
|
|
|
PDF格式 | **本条是由Drugfuture回溯的历史信息** |
| 5543408 |
2013/09/15 |
|
Y |
|
|
|
PDF格式 | **本条是由Drugfuture回溯的历史信息** |
与本品治疗等效的药品
>>>活性成分:MYCOPHENOLATE MOFETIL HYDROCHLORIDE; 剂型/给药途径:INJECTABLE;INJECTION; 规格:500MG/VIAL; 治疗等效代码:AP<<<
| 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 |
| 050758 |
001 |
NDA |
CELLCEPT |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
Yes |
Yes |
AP |
1998/08/12
|
ROCHE PALO |
| 203575 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2016/10/28
|
PH HEALTH |
| 204043 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2017/02/28
|
RISING |
| 203859 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2017/03/31
|
MYLAN LABS LTD |
| 204473 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2017/08/31
|
ZYDUS PHARMS |
| 212130 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2021/01/15
|
MEITHEAL |
| 216390 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2022/12/23
|
ONESOURCE SPECIALTY |
| 214283 |
001 |
ANDA |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
MYCOPHENOLATE MOFETIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
500MG/VIAL |
Prescription |
No |
No |
AP |
2023/06/01
|
BPI LABS |