FDA Drug Application (078627) for VENLAFAXINE HYDROCHLORIDE by SUN PHARM INDS INC

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Application Number078627
Product Number001
FormTABLET;ORAL
DosageEQ 25MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameVENLAFAXINE HYDROCHLORIDE
Active IngredientVENLAFAXINE HYDROCHLORIDE



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