美国FDA药品数据库（U.S. FDA Drugs Database）
符合检索条件的记录共 32 条
共 2 页，当前第 2 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 |
| CEFPROZIL |
065381 |
001 |
ANDA |
CEFPROZIL |
FOR SUSPENSION;ORAL |
125MG/5ML |
No
|
No
|
2007/01/30
|
2007/01/30
|
AUROBINDO PHARMA |
Prescription |
| CEFPROZIL |
065381 |
002 |
ANDA |
CEFPROZIL |
FOR SUSPENSION;ORAL |
250MG/5ML |
No
|
No
|
2007/01/30
|
2007/01/30
|
AUROBINDO PHARMA |
Prescription |
| CEFPROZIL |
065340 |
001 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
250MG |
No
|
No
|
2007/05/24
|
2007/05/24
|
AUROBINDO PHARMA |
Prescription |
| CEFPROZIL |
065340 |
002 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
500MG |
No
|
No
|
2007/05/24
|
2007/05/24
|
AUROBINDO PHARMA |
Prescription |
| CEFPROZIL |
065428 |
001 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
250MG |
No
|
No
|
2007/06/14
|
2007/06/14
|
WOCKHARDT |
Discontinued |
| CEFPROZIL |
065428 |
002 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
500MG |
No
|
No
|
2007/06/14
|
2007/06/14
|
WOCKHARDT |
Discontinued |
| CEFPROZIL |
065327 |
001 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
250MG |
No
|
No
|
2008/03/26
|
2008/03/26
|
APOTEX INC |
Prescription |
| CEFPROZIL |
065327 |
002 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
500MG |
No
|
No
|
2008/03/26
|
2008/03/26
|
APOTEX INC |
Prescription |
| CEFPROZIL |
065351 |
001 |
ANDA |
CEFPROZIL |
FOR SUSPENSION;ORAL |
125MG/5ML |
No
|
No
|
2012/02/29
|
2012/02/29
|
APOTEX INC |
Prescription |
| CEFPROZIL |
065351 |
002 |
ANDA |
CEFPROZIL |
FOR SUSPENSION;ORAL |
250MG/5ML |
No
|
No
|
2012/02/29
|
2012/02/29
|
APOTEX INC |
Prescription |
| CEFPROZIL |
090857 |
001 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
250MG |
No
|
No
|
2024/04/09
|
2024/04/09
|
ALKEM LABS LTD |
Prescription |
| CEFPROZIL |
090857 |
002 |
ANDA |
CEFPROZIL |
TABLET;ORAL |
500MG |
No
|
No
|
2024/04/09
|
2024/04/09
|
ALKEM LABS LTD |
Prescription |