"70934-223-30" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE, PLASTIC (70934-223-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-223-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70934-223-30)
Product NDC70934-223
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20190109
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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