HEXADROL |
012674 |
001 |
NDA |
DEXAMETHASONE |
ELIXIR;ORAL |
0.5MG/5ML |
No
|
No
|
1960/12/21
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
012675 |
004 |
NDA |
DEXAMETHASONE |
TABLET;ORAL |
0.5MG |
No
|
No
|
1962/04/20
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
012675 |
007 |
NDA |
DEXAMETHASONE |
TABLET;ORAL |
0.75MG |
No
|
No
|
1962/04/20
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
012675 |
009 |
NDA |
DEXAMETHASONE |
TABLET;ORAL |
1.5MG |
No
|
No
|
1962/04/20
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
012675 |
010 |
NDA |
DEXAMETHASONE |
TABLET;ORAL |
4MG |
No
|
No
|
1962/04/20
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
014694 |
002 |
NDA |
DEXAMETHASONE SODIUM PHOSPHATE |
INJECTABLE;INJECTION |
EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1964/12/04
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
014694 |
003 |
NDA |
DEXAMETHASONE SODIUM PHOSPHATE |
INJECTABLE;INJECTION |
EQ 10MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1964/12/04
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |
HEXADROL |
014694 |
004 |
NDA |
DEXAMETHASONE SODIUM PHOSPHATE |
INJECTABLE;INJECTION |
EQ 20MG PHOSPHATE/ML |
No
|
No
|
1964/12/04
|
Approved Prior to Jan 1, 1982
|
ASPEN GLOBAL INC |
Discontinued |