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"68071-3114-2" National Drug Code (NDC)

Fenofibrate 20 TABLET in 1 BOTTLE (68071-3114-2)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-3114-2
Package Description20 TABLET in 1 BOTTLE (68071-3114-2)
Product NDC68071-3114
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20140923
Marketing Category NameANDA
Application NumberANDA090715
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/68071-3114-2





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