IMODIUM |
017690 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
CAPSULE;ORAL |
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1976/12/28
|
Approved Prior to Jan 1, 1982
|
J AND J CONSUMER INC |
Discontinued |
IMODIUM |
017694 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
CAPSULE;ORAL |
2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1976/12/28
|
Approved Prior to Jan 1, 1982
|
J AND J CONSUMER INC |
Discontinued |
IMODIUM |
019037 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
SOLUTION;ORAL |
1MG/5ML |
No
|
No
|
1984/07/31
|
1984/07/31
|
JANSSEN PHARMS |
Discontinued |
IMODIUM A-D |
019487 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
SOLUTION;ORAL |
1MG/5ML |
Yes
|
Yes
|
1988/03/01
|
1988/03/01
|
KENVUE BRANDS |
Over-the-counter |
IMODIUM A-D |
019487 |
002 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
SUSPENSION;ORAL |
1MG/7.5ML |
Yes
|
Yes
|
1988/03/01
|
2004/07/08
|
KENVUE BRANDS |
Over-the-counter |
IMODIUM A-D |
019860 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
TABLET;ORAL |
2MG |
Yes
|
Yes
|
1989/11/22
|
1989/11/22
|
KENVUE BRANDS |
Over-the-counter |
IMODIUM MULTI-SYMPTOM RELIEF |
020606 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE; SIMETHICONE |
TABLET, CHEWABLE;ORAL |
2MG;125MG |
Yes
|
No
|
1997/06/26
|
1996/06/26
|
J AND J CONSUMER INC |
Discontinued |
IMODIUM A-D EZ CHEWS |
020448 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE |
TABLET, CHEWABLE;ORAL |
2MG |
Yes
|
No
|
1997/07/24
|
1997/07/24
|
J AND J CONSUMER INC |
Discontinued |
IMODIUM MULTI-SYMPTOM RELIEF |
021140 |
001 |
NDA |
LOPERAMIDE HYDROCHLORIDE; SIMETHICONE |
TABLET;ORAL |
2MG;125MG |
Yes
|
Yes
|
2000/11/30
|
2000/11/30
|
KENVUE BRANDS |
Over-the-counter |