FDA Drug Application (021235) for PROZAC WEEKLY by LILLY

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Application Number021235
Product Number001
FormCAPSULE, DELAYED REL PELLETS;ORAL
DosageEQ 90MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePROZAC WEEKLY
Active IngredientFLUOXETINE HYDROCHLORIDE



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