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"71335-2016-1" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (71335-2016-1)
(Bryant Ranch Prepack)

NDC Code71335-2016-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-2016-1)
Product NDC71335-2016
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130514
Marketing Category NameANDA
Application NumberANDA202856
ManufacturerBryant Ranch Prepack
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/71335-2016-1





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