美国FDA药品数据库（U.S. FDA Drugs Database）
符合检索条件的记录共 8 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 |
| PLERIXAFOR |
205182 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
DR REDDYS |
Prescription |
| PLERIXAFOR |
205197 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
TEVA PHARMS USA INC |
Prescription |
| PLERIXAFOR |
211901 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
MSN |
Prescription |
| PLERIXAFOR |
213672 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
EUGIA PHARMA |
Prescription |
| PLERIXAFOR |
215334 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
AMNEAL |
Prescription |
| PLERIXAFOR |
215698 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/24
|
2023/07/24
|
MEITHEAL |
Prescription |
| PLERIXAFOR |
208980 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2023/07/26
|
2023/07/26
|
ZYDUS PHARMS |
Discontinued |
| PLERIXAFOR |
206644 |
001 |
ANDA |
PLERIXAFOR |
SOLUTION;SUBCUTANEOUS |
24MG/1.2ML (20MG/ML) |
No
|
No
|
2024/05/03
|
2024/05/03
|
GLAND PHARMA LTD |
Prescription |