"0615-8270-39" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BLISTER PACK (0615-8270-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-8270-39
Package Description30 TABLET in 1 BLISTER PACK (0615-8270-39)
Product NDC0615-8270
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180720
Marketing Category NameANDA
Application NumberANDA210138
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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