FDA Drug Application (019507) for KERLONE by SANOFI AVENTIS US

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Application Number019507
Product Number001
FormTABLET;ORAL
Dosage10MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameKERLONE
Active IngredientBETAXOLOL HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient BETAXOLOL HYDROCHLORIDE6


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