FDA Drug Application (019839) for ZOLOFT by PFIZER

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Application Number019839
Product Number001
FormTABLET;ORAL
DosageEQ 50MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameZOLOFT
Active IngredientSERTRALINE HYDROCHLORIDE



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