FDA Drug Application (090669) for DULOXETINE HYDROCHLORIDE by IMPAX LABS INC

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Application Number090669
Product Number001
FormCAPSULE, DELAYED RELEASE; ORAL
DosageEQ 20MG BASE
Product Market Status Tentative Approval
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameDULOXETINE HYDROCHLORIDE
Active IngredientDULOXETINE HYDROCHLORIDE



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