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"68071-5101-9" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (68071-5101-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-5101-9
Package Description90 TABLET in 1 BOTTLE (68071-5101-9)
Product NDC68071-5101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20161215
Marketing Category NameANDA
Application NumberANDA208709
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/68071-5101-9





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