FDA Drug Application (070088) for IBU by BASF

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Application Number070088
Product Number001
FormTABLET;ORAL
Dosage600MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameIBU
Active IngredientIBUPROFEN

Active IngredientCount
List of drugs with Active Ingredient IBUPROFEN51


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