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"0074-3161-90" National Drug Code (NDC)

Trilipix 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-3161-90)
(AbbVie Inc.)

NDC Code0074-3161-90
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-3161-90)
Product NDC0074-3161
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrilipix
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20160912
Marketing Category NameNDA
Application NumberNDA022224
ManufacturerAbbVie Inc.
Substance NameFENOFIBRIC ACID
Strength45
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0074-3161-90





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