FdaApplication

NDA 019304

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date1993-12-31

Products (4)

ProductActive ingredientStrengthDosage form
LIPIDILFENOFIBRATE100MGCAPSULE;ORAL
TRICOR (MICRONIZED)FENOFIBRATE200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
TRICOR (MICRONIZED)FENOFIBRATE134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL
TRICOR (MICRONIZED)FENOFIBRATE67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE;ORAL

4 products