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"70934-591-30" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE, PLASTIC (70934-591-30)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)

NDC Code70934-591-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70934-591-30)
Product NDC70934-591
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200302
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA204019
ManufacturerDenton Pharma, Inc. dba Northwind Pharmaceuticals
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70934-591-30





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