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

Active IngredientCount
List of drugs with Active Ingredient DULOXETINE HYDROCHLORIDE2


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