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"70934-508-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-508-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-508-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-508-30)
Product NDC70934-508
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200121
Marketing Category NameANDA
Application NumberANDA204598
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-508-30





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