FdaApplication

ANDA 073459

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Identifiers

Properties

PropertyValue
applicant_nameOMNIVIUM PHARMACEUTICALS LLC
application_typeANDA
approval_date1993-10-31

Products (1)

ProductActive ingredientStrengthDosage form
CLEMASTINE FUMARATECLEMASTINE FUMARATE2.68MGTABLET;ORAL

1 product