FDA Drug Application (202660) for DUTASTERIDE by AUROLIFE PHARMA LLC

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Application Number202660
Product Number001
FormCAPSULE;ORAL
Dosage0.5MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameDUTASTERIDE
Active IngredientDUTASTERIDE



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