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- 50605 / DOSAGE - TABLET;ORAL - EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
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