FDA Drug Application (018932) for REVIA by TEVA WOMENS

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Application Number018932
Product Number001
FormTABLET;ORAL
Dosage50MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameREVIA
Active IngredientNALTREXONE HYDROCHLORIDE



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