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"16714-162-01" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (16714-162-01)
(NORTHSTAR RXLLC)

NDC Code16714-162-01
Package Description90 TABLET, FILM COATED in 1 BOTTLE (16714-162-01)
Product NDC16714-162
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210510
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerNORTHSTAR RXLLC
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-162-01





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