MONOPRIL |
019915 |
002 |
NDA |
FOSINOPRIL SODIUM |
TABLET;ORAL |
10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1991/05/16
|
1991/05/16
|
BRISTOL MYERS SQUIBB |
Discontinued |
MONOPRIL |
019915 |
003 |
NDA |
FOSINOPRIL SODIUM |
TABLET;ORAL |
20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1991/05/16
|
1991/05/16
|
BRISTOL MYERS SQUIBB |
Discontinued |
MONOPRIL |
019915 |
004 |
NDA |
FOSINOPRIL SODIUM |
TABLET;ORAL |
40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1991/05/16
|
1995/03/28
|
BRISTOL MYERS SQUIBB |
Discontinued |
MONOPRIL-HCT |
020286 |
001 |
NDA |
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
TABLET;ORAL |
20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1994/11/30
|
1994/11/30
|
BRISTOL MYERS SQUIBB |
Discontinued |
MONOPRIL-HCT |
020286 |
002 |
NDA |
FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
TABLET;ORAL |
10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1994/11/30
|
1994/11/30
|
BRISTOL MYERS SQUIBB |
Discontinued |