美国FDA药品数据库(U.S. FDA Drugs Database)
符合检索条件的记录共 121 条
共 7 页,当前第 5 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 |
AMPHETAMINE SULFATE |
212619 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2019/08/05
|
2019/08/05
|
GRANULES |
Prescription |
AMPHETAMINE SULFATE |
212619 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2019/08/05
|
2019/08/05
|
GRANULES |
Prescription |
AMPHETAMINE SULFATE |
212919 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2019/11/22
|
2019/11/22
|
BIONPHARMA |
Prescription |
AMPHETAMINE SULFATE |
212919 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2019/11/22
|
2019/11/22
|
BIONPHARMA |
Prescription |
AMPHETAMINE SULFATE |
212582 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/02/04
|
2020/02/04
|
SANALUZ |
Prescription |
AMPHETAMINE SULFATE |
212582 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/02/04
|
2020/02/04
|
SANALUZ |
Prescription |
AMPHETAMINE SULFATE |
211861 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/03/11
|
2020/03/11
|
PRINSTON INC |
Prescription |
AMPHETAMINE SULFATE |
211861 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/03/11
|
2020/03/11
|
PRINSTON INC |
Prescription |
AMPHETAMINE SULFATE |
212901 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/05/22
|
2020/05/22
|
SENORES PHARMS |
Prescription |
AMPHETAMINE SULFATE |
212901 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/05/22
|
2020/05/22
|
SENORES PHARMS |
Prescription |
AMPHETAMINE SULFATE |
213898 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/07/14
|
2020/07/14
|
DR REDDYS LABS SA |
Discontinued |
AMPHETAMINE SULFATE |
213898 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/07/14
|
2020/07/14
|
DR REDDYS LABS SA |
Discontinued |
AMPHETAMINE SULFATE |
213763 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/08/24
|
2020/08/24
|
NOVAST LABS |
Discontinued |
AMPHETAMINE SULFATE |
213763 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/08/24
|
2020/08/24
|
NOVAST LABS |
Discontinued |
AMPHETAMINE SULFATE |
213720 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/10/27
|
2020/10/27
|
ALKEM LABS LTD |
Prescription |
AMPHETAMINE SULFATE |
213720 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/10/27
|
2020/10/27
|
ALKEM LABS LTD |
Prescription |
AMPHETAMINE SULFATE |
213980 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2020/10/27
|
2020/10/27
|
EPIC PHARMA LLC |
Prescription |
AMPHETAMINE SULFATE |
213980 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2020/10/27
|
2020/10/27
|
EPIC PHARMA LLC |
Prescription |
AMPHETAMINE SULFATE |
213583 |
001 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
No
|
No
|
2021/01/22
|
2021/01/22
|
SPECGX LLC |
Prescription |
AMPHETAMINE SULFATE |
213583 |
002 |
ANDA |
AMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
No
|
No
|
2021/01/22
|
2021/01/22
|
SPECGX LLC |
Prescription |