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"16714-738-01" National Drug Code (NDC)

Fenofibrate 90 TABLET, COATED in 1 BOTTLE (16714-738-01)
(NorthStar Rx LLC)

NDC Code16714-738-01
Package Description90 TABLET, COATED in 1 BOTTLE (16714-738-01)
Product NDC16714-738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20170715
Marketing Category NameANDA
Application NumberANDA205118
ManufacturerNorthStar Rx LLC
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-738-01





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