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

Back to FDA Applications sponsored by AUROLIFE PHARMA LLC

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

Active IngredientCount
List of drugs with Active Ingredient DUTASTERIDE4


Back to FDA Applications sponsored by AUROLIFE PHARMA LLC