FDA Drug Application (018754) for ORUDIS by WYETH AYERST

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Application Number018754
Product Number001
FormCAPSULE;ORAL
Dosage25MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameORUDIS
Active IngredientKETOPROFEN

Active IngredientCount
List of drugs with Active Ingredient KETOPROFEN6


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