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

Active IngredientCount
List of drugs with Active Ingredient FLUOXETINE HYDROCHLORIDE8


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