"68071-4983-3" National Drug Code (NDC)

Fenofibrate 30 TABLET, COATED in 1 BOTTLE (68071-4983-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4983-3
Package Description30 TABLET, COATED in 1 BOTTLE (68071-4983-3)
Product NDC68071-4983
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20160505
Marketing Category NameANDA
Application NumberANDA205118
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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