
USFDA APPLICATION NUMBER - 20496 / DOSAGE - TABLET;ORAL - 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| GLIMEPIRIDE(UNII: 6KY687524K) (GLIMEPIRIDE - UNII:6KY687524K) | GLIMEPIRIDE | 4mg | 2mg | 1mg |
Inactive Ingredients
| Ingredient Name | Sanofi-Aventis U.S. LLC |
|---|---|
| ALUMINUM OXIDE(LMI26O6933) | |
| FD&C BLUE NO. 2(L06K8R7DQK) | |
| FERRIC OXIDE RED(1K09F3G675) | |
| FERRIC OXIDE YELLOW(EX438O2MRT) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| POVIDONE, UNSPECIFIED(FZ989GH94E) | |
| SODIUM STARCH GLYCOLATE TYPE A CORN(AG9B65PV6B) |