FDA Drug Application (202179) for PREDNISOLONE SODIUM PHOSPHATE by MYLAN PHARMS INC

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Application Number202179
Product Number001
FormTABLET, ORALLY DISINTEGRATING;ORAL
DosageEQ 10MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NamePREDNISOLONE SODIUM PHOSPHATE
Active IngredientPREDNISOLONE SODIUM PHOSPHATE



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