FDA Drug Application (201748) for FENOFIBRATE by SUN PHARM INDS LTD

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Application Number201748
Product Number001
FormCAPSULE;ORAL
Dosage43MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameFENOFIBRATE
Active IngredientFENOFIBRATE

Active IngredientCount
List of drugs with Active Ingredient FENOFIBRATE9


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