美国FDA药品数据库（U.S. FDA Drugs Database）
符合检索条件的记录共 26 条
共 2 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 |
| NABUMETONE |
075189 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2000/05/26
|
2000/05/26
|
IMPAX LABS INC |
Discontinued |
| NABUMETONE |
075189 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2000/05/26
|
2001/09/24
|
IMPAX LABS INC |
Discontinued |
| NABUMETONE |
075179 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2000/06/06
|
2000/06/06
|
COPLEY PHARM |
Discontinued |
| NABUMETONE |
075280 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2002/02/25
|
2002/02/25
|
CHARTWELL RX |
Prescription |
| NABUMETONE |
075280 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2002/02/25
|
2002/02/25
|
CHARTWELL RX |
Prescription |
| NABUMETONE |
075590 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2002/02/25
|
2002/02/25
|
EPIC PHARMA LLC |
Discontinued |
| NABUMETONE |
075590 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2002/02/25
|
2002/02/25
|
EPIC PHARMA LLC |
Discontinued |
| NABUMETONE |
076009 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2003/01/24
|
2003/01/24
|
CHARTWELL MOLECULES |
Prescription |
| NABUMETONE |
076009 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2003/01/24
|
2003/01/24
|
CHARTWELL MOLECULES |
Prescription |
| NABUMETONE |
078671 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2008/03/07
|
2008/03/07
|
INVAGEN PHARMS |
Prescription |
| NABUMETONE |
078671 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
Yes
|
2008/03/07
|
2008/03/07
|
INVAGEN PHARMS |
Prescription |
| NABUMETONE |
078420 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2008/09/24
|
2008/09/24
|
SCIEGEN PHARMS INC |
Prescription |
| NABUMETONE |
078420 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2008/09/24
|
2008/09/24
|
SCIEGEN PHARMS INC |
Prescription |
| NABUMETONE |
079093 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2009/02/27
|
2009/02/27
|
OXFORD PHARMS |
Discontinued |
| NABUMETONE |
079093 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2009/02/27
|
2009/02/27
|
OXFORD PHARMS |
Discontinued |
| NABUMETONE |
090516 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2010/07/12
|
2010/07/12
|
AUROBINDO PHARMA USA |
Discontinued |
| NABUMETONE |
090516 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2010/07/12
|
2010/07/12
|
AUROBINDO PHARMA USA |
Discontinued |
| NABUMETONE |
090445 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2011/01/12
|
2011/01/12
|
ANNORA PHARMA |
Prescription |
| NABUMETONE |
090445 |
002 |
ANDA |
NABUMETONE |
TABLET;ORAL |
750MG |
No
|
No
|
2011/01/12
|
2011/01/12
|
ANNORA PHARMA |
Prescription |
| NABUMETONE |
091083 |
001 |
ANDA |
NABUMETONE |
TABLET;ORAL |
500MG |
No
|
No
|
2011/06/13
|
2011/06/13
|
WATSON LABS |
Prescription |