FDA Drug Application (077338) for IBUPROFEN by P AND L DEV LLC

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Application Number077338
Product Number001
FormCAPSULE;ORAL
DosageEQ 200MG FREE ACID AND POTASSIUM SALT
Product Market Status Over The Counter
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameIBUPROFEN
Active IngredientIBUPROFEN

Active IngredientCount
List of drugs with Active Ingredient IBUPROFEN51


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