FDA Drug Application (022059) for TYKERB by NOVARTIS PHARMS CORP

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Application Number022059
Product Number001
FormTABLET;ORAL
DosageEQ 250MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameTYKERB
Active IngredientLAPATINIB DITOSYLATE



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