FDA Drug Application (020459) for REVEX by EUROHLTH INTL SARL

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Application Number020459
Product Number001
FormINJECTABLE;INJECTION
DosageEQ 0.1MG BASE/ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameREVEX
Active IngredientNALMEFENE HYDROCHLORIDE



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