美国FDA药品数据库（U.S. FDA Drugs Database）
符合检索条件的记录共 191 条
共 10 页，当前第 10 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 |
| RISPERIDONE |
078036 |
001 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
0.25MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
078036 |
002 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
0.5MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
078036 |
003 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
1MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
078036 |
004 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
2MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
078036 |
005 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
3MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
078036 |
006 |
ANDA |
RISPERIDONE |
TABLET;ORAL |
4MG |
No
|
No
|
2014/03/10
|
2014/03/10
|
SUN PHARM INDS INC |
Discontinued |
| RISPERIDONE |
202386 |
001 |
ANDA |
RISPERIDONE |
SOLUTION;ORAL |
1MG/ML |
No
|
No
|
2015/01/12
|
2015/01/12
|
CHARTWELL MOLECULAR |
Prescription |
| RISPERIDONE |
214068 |
001 |
ANDA |
RISPERIDONE |
INJECTABLE;INTRAMUSCULAR |
12.5MG/VIAL |
No
|
No
|
2023/12/05
|
2023/12/05
|
TEVA PHARMS USA INC |
Prescription |
| RISPERIDONE |
214068 |
002 |
ANDA |
RISPERIDONE |
INJECTABLE;INTRAMUSCULAR |
25MG/VIAL |
No
|
No
|
2023/12/05
|
2023/12/05
|
TEVA PHARMS USA INC |
Prescription |
| RISPERIDONE |
214068 |
003 |
ANDA |
RISPERIDONE |
INJECTABLE;INTRAMUSCULAR |
37.5MG/VIAL |
No
|
No
|
2023/12/05
|
2023/12/05
|
TEVA PHARMS USA INC |
Prescription |
| RISPERIDONE |
214068 |
004 |
ANDA |
RISPERIDONE |
INJECTABLE;INTRAMUSCULAR |
50MG/VIAL |
No
|
No
|
2023/12/05
|
2023/12/05
|
TEVA PHARMS USA INC |
Prescription |