
USFDA APPLICATION NUMBER - 50605 / DOSAGE - TABLET;ORAL - EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| CEFUROXIME AXETIL(UNII: Z49QDT0J8Z) (CEFUROXIME - UNII:O1R9FJ93ED) | CEFUROXIME | 250mg in 5 | 125mg in 5 | 250mg |
Inactive Ingredients
| Ingredient Name | GlaxoSmithKline LLC |
|---|---|
| ACESULFAME POTASSIUM(23OV73Q5G9) | |
| ASPARTAME(Z0H242BBR1) | |
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
| CROSCARMELLOSE SODIUM(M28OL1HH48) | |
| HYPROMELLOSES(3NXW29V3WO) | |
| METHYLPARABEN(A2I8C7HI9T) | |
| POVIDONE K30(U725QWY32X) | |
| PROPYLENE GLYCOL(6DC9Q167V3) | |
| PROPYLPARABEN(Z8IX2SC1OH) | |
| SILICON DIOXIDE(ETJ7Z6XBU4) | |
| SODIUM BENZOATE(OJ245FE5EU) | |
| SODIUM LAURYL SULFATE(368GB5141J) | |
| STEARIC ACID(4ELV7Z65AP) | |
| SUCROSE(C151H8M554) | |
| TITANIUM DIOXIDE(15FIX9V2JP) | |
| XANTHAN GUM(TTV12P4NEE) |