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 |
| 2012/02/02 |
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 |
| 2022/06/21 |
SUPPL-26(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/11/04 |
SUPPL-25(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2020/12/04 |
SUPPL-22(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
PRIORITY
|
|
|
| 2019/08/12 |
SUPPL-19(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
STANDARD
|
|
|
| 2019/07/01 |
SUPPL-20(补充) |
Approval |
Labeling-Package Insert |
901 REQUIRED
|
|
|
| 2018/02/09 |
SUPPL-18(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/08/10 |
SUPPL-17(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/01/18 |
SUPPL-16(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2017/01/18 |
SUPPL-15(补充) |
Approval |
Labeling-Package Insert |
901 REQUIRED
|
|
|
| 2015/08/28 |
SUPPL-10(补充) |
Approval |
Labeling-Medication Guide |
901 REQUIRED
|
|
|
| 2015/04/27 |
SUPPL-9(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/09/19 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2014/02/12 |
SUPPL-6(补充) |
Approval |
Labeling-Medication Guide |
STANDARD
|
|
|
| 2013/10/17 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/07/19 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/04/10 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/02/11 |
SUPPL-3(补充) |
Approval |
Labeling-Container/Carton Labels,Labeling-Medication Guide |
STANDARD
|
|
|
| 2012/10/18 |
SUPPL-2(补充) |
Approval |
Labeling-Medication Guide |
UNKNOWN
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
>>>活性成分:METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE; 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL; 规格:500MG;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 |
| 202270 |
001 |
NDA |
JANUMET XR |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
500MG;EQ 50MG BASE |
Prescription |
Yes |
No |
AB |
2012/02/02
|
MSD SUB MERCK |
| 204144 |
001 |
ANDA |
SITAGLIPTIN AND METFORMIN HYDROCHLORIDE |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
500MG;EQ 50MG BASE |
Discontinued |
No |
No |
AB |
2025/06/04
|
PH HEALTH |
>>>活性成分:METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE; 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL; 规格:1GM;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 |
| 202270 |
002 |
NDA |
JANUMET XR |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
1GM;EQ 50MG BASE |
Prescription |
Yes |
No |
AB |
2012/02/02
|
MSD SUB MERCK |
| 204144 |
002 |
ANDA |
SITAGLIPTIN AND METFORMIN HYDROCHLORIDE |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
1GM;EQ 50MG BASE |
Discontinued |
No |
No |
AB |
2025/06/04
|
PH HEALTH |
>>>活性成分:METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE; 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL; 规格:1GM;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 |
| 202270 |
003 |
NDA |
JANUMET XR |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
1GM;EQ 100MG BASE |
Prescription |
Yes |
Yes |
AB |
2012/02/02
|
MSD SUB MERCK |
| 204144 |
003 |
ANDA |
SITAGLIPTIN AND METFORMIN HYDROCHLORIDE |
METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE |
TABLET, EXTENDED RELEASE;ORAL |
1GM;EQ 100MG BASE |
Discontinued |
No |
No |
AB |
2025/06/04
|
PH HEALTH |