"70934-298-60" National Drug Code (NDC)

Fenofibrate 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-298-60)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-298-60
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-298-60)
Product NDC70934-298
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190301
Marketing Category NameANDA
Application NumberANDA076433
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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