"68071-2115-3" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (68071-2115-3)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-2115-3
Package Description30 TABLET in 1 BOTTLE (68071-2115-3)
Product NDC68071-2115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20160209
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021656
ManufacturerNuCare Pharmaceuticals, Inc.
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/68071-2115-3