FdaApplication

NDA 020719

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Identifiers

Properties

PropertyValue
applicant_nameSANKYO USA CORP
application_typeNDA
approval_date1997-01-29

Products (3)

ProductActive ingredientStrengthDosage form
PRELAYTROGLITAZONE200MGTABLET;ORAL
PRELAYTROGLITAZONE300MGTABLET;ORAL
PRELAYTROGLITAZONE400MGTABLET;ORAL

3 products