FDA Drug Application (090778) for DULOXETINE HYDROCHLORIDE by AUROBINDO PHARMA LTD

Back to FDA Applications sponsored by AUROBINDO PHARMA LTD

Application Number090778
Product Number001
FormCAPSULE, DELAYED REL PELLETS;ORAL
DosageEQ 20MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameDULOXETINE HYDROCHLORIDE
Active IngredientDULOXETINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient DULOXETINE HYDROCHLORIDE2


Back to FDA Applications sponsored by AUROBINDO PHARMA LTD