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

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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



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