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



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