VOLTAREN |
019201 |
001 |
NDA |
DICLOFENAC SODIUM |
TABLET, DELAYED RELEASE;ORAL |
25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1988/07/28
|
1988/07/28
|
NOVARTIS |
Discontinued |
VOLTAREN |
019201 |
002 |
NDA |
DICLOFENAC SODIUM |
TABLET, DELAYED RELEASE;ORAL |
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1988/07/28
|
1988/07/28
|
NOVARTIS |
Discontinued |
VOLTAREN |
019201 |
003 |
NDA |
DICLOFENAC SODIUM |
TABLET, DELAYED RELEASE;ORAL |
75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1988/07/28
|
1988/07/28
|
NOVARTIS |
Discontinued |
VOLTAREN |
020037 |
001 |
NDA |
DICLOFENAC SODIUM |
SOLUTION/DROPS;OPHTHALMIC |
0.1% |
Yes
|
No
|
1991/03/28
|
1991/03/28
|
NOVARTIS |
Discontinued |
VOLTAREN-XR |
020254 |
001 |
NDA |
DICLOFENAC SODIUM |
TABLET, EXTENDED RELEASE;ORAL |
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1996/03/08
|
1996/03/08
|
NOVARTIS |
Discontinued |
VOLTAREN ARTHRITIS PAIN |
022122 |
001 |
NDA |
DICLOFENAC SODIUM |
GEL;TOPICAL |
1% |
Yes
|
Yes
|
2007/10/17
|
2007/10/17
|
HALEON US HOLDINGS |
Over-the-counter |