FDA Drug Application (074978) for IBUPROFEN by ACTAVIS MID ATLANTIC

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Application Number074978
Product Number001
FormSUSPENSION;ORAL
Dosage100MG/5ML
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameIBUPROFEN
Active IngredientIBUPROFEN

Active IngredientCount
List of drugs with Active Ingredient IBUPROFEN51


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