UNIRETIC |
020729 |
001 |
NDA |
HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
TABLET;ORAL |
12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1997/06/27
|
1997/06/27
|
UCB INC |
Discontinued |
UNIRETIC |
020729 |
002 |
NDA |
HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
TABLET;ORAL |
25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1997/06/27
|
1997/06/27
|
UCB INC |
Discontinued |
UNIRETIC |
020729 |
003 |
NDA |
HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
TABLET;ORAL |
12.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1997/06/27
|
2002/02/14
|
UCB INC |
Discontinued |