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"68382-230-16" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (68382-230-16)
(Zydus Pharmaceuticals USA Inc)

NDC Code68382-230-16
Package Description90 TABLET in 1 BOTTLE (68382-230-16)
Product NDC68382-230
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20041105
End Marketing Date20190126
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021656
ManufacturerZydus Pharmaceuticals USA 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/68382-230-16





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