FDA Drug Application (201951) for DOXEPIN HYDROCHLORIDE by ACTAVIS ELIZABETH

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Application Number201951
Product Number001
FormTABLET;ORAL
DosageEQ 3MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameDOXEPIN HYDROCHLORIDE
Active IngredientDOXEPIN HYDROCHLORIDE



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