FDA Drug Application (019807) for KERLEDEX by SANOFI AVENTIS US

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Application Number019807
Product Number001
FormTABLET;ORAL
Dosage5MG;12.5MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameKERLEDEX
Active IngredientBETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE

Active IngredientCount
List of drugs with Active Ingredient BETAXOLOL HYDROCHLORIDE6
List of drugs with Active Ingredient CHLORTHALIDONE14


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