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 |
| 2001/08/15 |
ORIG-1(原始申请) |
Approval |
Type 4 - New Combination |
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 |
| 2023/02/13 |
SUPPL-15(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/09/10 |
SUPPL-21(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/03/04 |
SUPPL-20(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2019/10/07 |
SUPPL-19(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2018/09/18 |
SUPPL-17(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2018/09/18 |
SUPPL-16(补充) |
Approval |
REMS - PROPOSAL - D-N-A |
N/A
|
|
|
| 2017/08/29 |
SUPPL-14(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/12/16 |
SUPPL-13(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/12/16 |
SUPPL-12(补充) |
Approval |
Labeling-Medication Guide,Labeling-Package Insert |
STANDARD
|
|
|
| 2016/12/16 |
SUPPL-10(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2013/10/18 |
SUPPL-8(补充) |
Approval |
Labeling,Labeling-Package Insert |
901 REQUIRED
|
|
|
| 2011/06/22 |
SUPPL-5(补充) |
Approval |
Labeling-Package Insert |
UNKNOWN
|
|
|
| 2009/09/09 |
SUPPL-3(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2004/04/16 |
SUPPL-1(补充) |
Approval |
Labeling |
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 |
RE39221 |
2011/08/09 |
Y |
Y |
U-55 |
|
|
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:ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE; 剂型/给药途径:TABLET;ORAL; 规格:325MG;37.5MG; 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 |
| 021123 |
001 |
NDA |
ULTRACET |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Discontinued |
Yes |
No |
AB |
2001/08/15
|
JANSSEN PHARMS |
| 077184 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Discontinued |
No |
No |
AB |
2005/12/16
|
SUN PHARM INDS INC |
| 077858 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
No |
AB |
2008/09/26
|
RISING |
| 090485 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
Yes |
AB |
2009/12/09
|
AMNEAL PHARMS |
| 202076 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
No |
AB |
2012/03/30
|
ALKEM LABS LTD |
| 090460 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
No |
AB |
2012/09/06
|
ZYDUS PHARMS USA INC |
| 201952 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
No |
AB |
2012/12/14
|
MICRO LABS LTD INDIA |
| 207152 |
001 |
ANDA |
TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE |
TABLET;ORAL |
325MG;37.5MG |
Prescription |
No |
No |
AB |
2017/03/22
|
AUROBINDO PHARMA |