FDA Drug Application (078769) for OXYCODONE HYDROCHLORIDE AND IBUPROFEN by ACTAVIS ELIZABETH

Back to FDA Applications sponsored by ACTAVIS ELIZABETH

Application Number078769
Product Number001
FormTABLET;ORAL
Dosage400MG;5MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameOXYCODONE HYDROCHLORIDE AND IBUPROFEN
Active IngredientIBUPROFEN; OXYCODONE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient IBUPROFEN51
List of drugs with Active Ingredient OXYCODONE HYDROCHLORIDE27


Back to FDA Applications sponsored by ACTAVIS ELIZABETH