FdaApplication

ANDA 040586

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Identifiers

Properties

PropertyValue
applicant_nameOXFORD PHARMACEUTICALS LLC
application_typeANDA
approval_date2005-02-24

Products (2)

ProductActive ingredientStrengthDosage form
PRIMIDONEPRIMIDONE50MGTABLET;ORAL
PRIMIDONEPRIMIDONE250MGTABLET;ORAL

2 products