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"0074-9642-10" National Drug Code (NDC)

Trilipix 3 BLISTER PACK in 1 CARTON (0074-9642-10) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
(AbbVie Inc.)

NDC Code0074-9642-10
Package Description3 BLISTER PACK in 1 CARTON (0074-9642-10) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC0074-9642
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrilipix
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20081215
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/0074-9642-10





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