FDA Drug Application (075189) for NABUMETONE by IMPAX LABS INC

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Application Number075189
Product Number001
FormTABLET;ORAL
Dosage500MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameNABUMETONE
Active IngredientNABUMETONE



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