FDA Drug Application (050791) for MYFORTIC by NOVARTIS

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Application Number050791
Product Number001
FormTABLET, DELAYED RELEASE;ORAL
Dosage180MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameMYFORTIC
Active IngredientMYCOPHENOLIC ACID



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