美国FDA药品数据库(U.S. FDA Drugs Database)
符合检索条件的记录共 69 条
共 4 页,当前第 4 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 |
PEMETREXED DISODIUM |
214436 |
002 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
No
|
No
|
2022/08/18
|
2022/08/18
|
BAXTER HLTHCARE CORP |
Prescription |
PEMETREXED DISODIUM |
215479 |
001 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 100MG BASE/VIAL |
No
|
No
|
2022/12/13
|
2022/12/13
|
MEITHEAL |
Prescription |
PEMETREXED DISODIUM |
215479 |
002 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
No
|
No
|
2022/12/13
|
2022/12/13
|
MEITHEAL |
Prescription |
PEMETREXED DISODIUM |
215479 |
003 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 750MG BASE/VIAL |
No
|
No
|
2022/12/13
|
2022/12/13
|
MEITHEAL |
Prescription |
PEMETREXED DISODIUM |
215479 |
004 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 1GM BASE/VIAL |
No
|
No
|
2022/12/13
|
2022/12/13
|
MEITHEAL |
Prescription |
PEMETREXED DISODIUM |
203628 |
001 |
ANDA |
PEMETREXED DISODIUM |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
No
|
No
|
2023/03/10
|
2023/03/10
|
MYLAN LABS LTD |
Discontinued |
PEMETREXED |
215179 |
001 |
NDA |
PEMETREXED |
SOLUTION;INTRAVENOUS |
100MG/10ML |
No
|
No
|
2023/05/22
|
--
|
SHILPA MEDICARE LTD |
Prescription |
PEMETREXED |
215179 |
002 |
NDA |
PEMETREXED |
SOLUTION;INTRAVENOUS |
500MG/50ML |
No
|
No
|
2023/05/22
|
--
|
SHILPA MEDICARE LTD |
Prescription |
PEMETREXED |
215179 |
003 |
NDA |
PEMETREXED |
SOLUTION;INTRAVENOUS |
1000MG/100ML |
No
|
No
|
2023/05/22
|
--
|
SHILPA MEDICARE LTD |
Prescription |