"70934-567-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-567-30)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)

NDC Code70934-567-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-567-30)
Product NDC70934-567
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200227
Marketing Category NameANDA
Application NumberANDA204598
ManufacturerDenton Pharma, Inc. dba Northwind Pharmaceuticals
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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