FDA Drug Application (075274) for NALTREXONE HYDROCHLORIDE by ELITE LABS

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Application Number075274
Product Number001
FormTABLET;ORAL
Dosage50MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameNALTREXONE HYDROCHLORIDE
Active IngredientNALTREXONE HYDROCHLORIDE



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