FDA Drug Application (020429) for ORUDIS KT by WYETH CONS

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Application Number020429
Product Number001
FormTABLET;ORAL
Dosage12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameORUDIS KT
Active IngredientKETOPROFEN

Active IngredientCount
List of drugs with Active Ingredient KETOPROFEN6


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