ELOXATIN |
021492 |
001 |
NDA |
OXALIPLATIN |
INJECTABLE;INTRAVENOUS |
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
2002/08/09
|
2002/08/09
|
SANOFI AVENTIS US |
Discontinued |
ELOXATIN |
021492 |
002 |
NDA |
OXALIPLATIN |
INJECTABLE;INTRAVENOUS |
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
2002/08/09
|
2002/08/09
|
SANOFI AVENTIS US |
Discontinued |
ELOXATIN |
021759 |
001 |
NDA |
OXALIPLATIN |
INJECTABLE;INTRAVENOUS |
50MG/10ML (5MG/ML) |
Yes
|
No
|
2005/01/31
|
2005/01/31
|
SANOFI AVENTIS US |
Discontinued |
ELOXATIN |
021759 |
002 |
NDA |
OXALIPLATIN |
INJECTABLE;INTRAVENOUS |
100MG/20ML (5MG/ML) |
Yes
|
No
|
2005/01/31
|
2005/01/31
|
SANOFI AVENTIS US |
Discontinued |
ELOXATIN |
021759 |
003 |
NDA |
OXALIPLATIN |
INJECTABLE;INTRAVENOUS |
200MG/40ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
2005/01/31
|
2006/11/17
|
SANOFI AVENTIS US |
Discontinued |