| TENUATE |
011722 |
002 |
NDA |
DIETHYLPROPION HYDROCHLORIDE |
TABLET;ORAL |
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1959/08/06
|
Approved Prior to Jan 1, 1982
|
NOSTRUM LABS INC |
Discontinued |
| TENUATE DOSPAN |
012546 |
001 |
NDA |
DIETHYLPROPION HYDROCHLORIDE |
TABLET, EXTENDED RELEASE;ORAL |
75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1960/11/17
|
Approved Prior to Jan 1, 1982
|
NOSTRUM LABS INC |
Discontinued |
| TENUATE |
017668 |
001 |
NDA |
DIETHYLPROPION HYDROCHLORIDE |
TABLET;ORAL |
25MG |
No
|
No
|
1975/03/20
|
Approved Prior to Jan 1, 1982
|
SANOFI AVENTIS US |
Discontinued |
| TENUATE |
017669 |
001 |
NDA |
DIETHYLPROPION HYDROCHLORIDE |
TABLET, EXTENDED RELEASE;ORAL |
75MG |
No
|
No
|
1975/03/20
|
Approved Prior to Jan 1, 1982
|
SANOFI AVENTIS US |
Discontinued |