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"68071-1601-9" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (68071-1601-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-1601-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68071-1601-9)
Product NDC68071-1601
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060510
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-1601-9





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