USFDA APPLICATION NUMBER - 50564 / DOSAGE - TABLET;ORAL - 250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
amoxicillin(UNII: 804826J2HU) (amoxicillin - UNII:804826J2HU) | amoxicillin | 500mg |
clavulanate potassium(UNII: Q42OMW3AT8) (clavulanic acid - UNII:23521W1S24) | clavulanate potassium | 125mg |
Inactive Ingredients
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