FDA Drug Application (074024) for KETOPROFEN by AUROLIFE PHARMA LLC

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Application Number074024
Product Number001
FormCAPSULE;ORAL
Dosage50MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameKETOPROFEN
Active IngredientKETOPROFEN

Active IngredientCount
List of drugs with Active Ingredient KETOPROFEN6


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