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"0615-8165-39" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BLISTER PACK (0615-8165-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-8165-39
Package Description30 TABLET in 1 BLISTER PACK (0615-8165-39)
Product NDC0615-8165
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180711
End Marketing Date20201130
Marketing Category NameANDA
Application NumberANDA204019
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0615-8165-39





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