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"68682-495-90" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (68682-495-90)
(Oceanside Pharmaceuticals)

NDC Code68682-495-90
Package Description90 TABLET in 1 BOTTLE (68682-495-90)
Product NDC68682-495
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20210316
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022118
ManufacturerOceanside Pharmaceuticals
Substance NameFENOFIBRATE
Strength120
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68682-495-90





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