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"0093-2061-98" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (0093-2061-98)
(Teva Pharmaceuticals USA Inc)

NDC Code0093-2061-98
Package Description90 TABLET in 1 BOTTLE (0093-2061-98)
Product NDC0093-2061
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20041105
End Marketing Date20181231
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021656
ManufacturerTeva Pharmaceuticals USA Inc
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-2061-98





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