FDA Drug Application (072395) for FENOPROFEN CALCIUM by AUROLIFE PHARMA LLC

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Application Number072395
Product Number001
FormCAPSULE;ORAL
DosageEQ 300MG BASE
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameFENOPROFEN CALCIUM
Active IngredientFENOPROFEN CALCIUM

Active IngredientCount
List of drugs with Active Ingredient FENOPROFEN CALCIUM2


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