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"71335-0872-3" National Drug Code (NDC)

Fenofibrate 28 TABLET, FILM COATED in 1 BOTTLE (71335-0872-3)
(Bryant Ranch Prepack)

NDC Code71335-0872-3
Package Description28 TABLET, FILM COATED in 1 BOTTLE (71335-0872-3)
Product NDC71335-0872
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180601
Marketing Category NameANDA
Application NumberANDA200884
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/71335-0872-3





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