FdaApplication

NDA 021203

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date2001-09-04

Products (2)

ProductActive ingredientStrengthDosage form
TRICORFENOFIBRATE54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL
TRICORFENOFIBRATE160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET;ORAL

2 products