美国FDA药品数据库(U.S. FDA Drugs Database)
符合检索条件的记录共 10 条
共 1 页,当前第 1 页
商品名 |
申请号 |
产品号 |
申请类型 |
活性成分 |
剂型/给药途径 |
规格/剂量 |
RLD |
RS |
申请号原始批准/暂定批准日期 |
产品号批准日期 |
申请人 |
市场状态 |
CEFIXIME |
204835 |
001 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
100MG/5ML |
No
|
No
|
2015/04/14
|
2015/04/14
|
AUROBINDO PHARMA LTD |
Prescription |
CEFIXIME |
204835 |
002 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
200MG/5ML |
No
|
No
|
2015/04/14
|
2015/04/14
|
AUROBINDO PHARMA LTD |
Prescription |
CEFIXIME |
206938 |
001 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
100MG/5ML |
No
|
No
|
2017/02/06
|
2017/02/06
|
BELCHER |
Prescription |
CEFIXIME |
206938 |
002 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
200MG/5ML |
No
|
No
|
2017/02/06
|
2017/02/06
|
BELCHER |
Prescription |
CEFIXIME |
206939 |
001 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
500MG/5ML |
No
|
No
|
2017/02/06
|
2017/02/06
|
BELCHER |
Prescription |
CEFIXIME |
206144 |
001 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
100MG/5ML |
No
|
No
|
2017/11/17
|
2017/11/17
|
CHARTWELL RX |
Discontinued |
CEFIXIME |
206144 |
002 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
200MG/5ML |
No
|
No
|
2017/11/17
|
2017/11/17
|
CHARTWELL RX |
Discontinued |
CEFIXIME |
210574 |
001 |
ANDA |
CEFIXIME |
CAPSULE;ORAL |
400MG |
No
|
No
|
2018/10/09
|
2018/10/09
|
ALKEM LABS LTD |
Prescription |
CEFIXIME |
211775 |
001 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
100MG/5ML |
No
|
No
|
2021/02/19
|
2021/02/19
|
ALKEM LABS LTD |
Prescription |
CEFIXIME |
211775 |
002 |
ANDA |
CEFIXIME |
FOR SUSPENSION;ORAL |
200MG/5ML |
No
|
No
|
2021/02/19
|
2021/02/19
|
ALKEM LABS LTD |
Prescription |