FDA Drug Application (072191) for CLOFIBRATE by SANDOZ

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Application Number072191
Product Number001
FormCAPSULE;ORAL
Dosage500MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameCLOFIBRATE
Active IngredientCLOFIBRATE

Active IngredientCount
List of drugs with Active Ingredient CLOFIBRATE2


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