"16714-739-01" National Drug Code (NDC)

Fenofibrate 90 CAPSULE in 1 BOTTLE, PLASTIC (16714-739-01)
(Northstar Rx LLC)

NDC Code16714-739-01
Package Description90 CAPSULE in 1 BOTTLE, PLASTIC (16714-739-01)
Product NDC16714-739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20170821
Marketing Category NameANDA
Application NumberANDA207378
ManufacturerNorthstar Rx LLC
Substance NameFENOFIBRATE
Strength67
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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