FdaApplication

NDA 018675

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Identifiers

Properties

PropertyValue
applicant_nameNOVARTIS PHARMACEUTICALS CORP
application_typeNDA
approval_date1985-06-28

Products (1)

ProductActive ingredientStrengthDosage form
TAVISTCLEMASTINE FUMARATEEQ 0.5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SYRUP;ORAL

1 product