"69097-458-05" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (69097-458-05)
(Cipla USA Inc.)

NDC Code69097-458-05
Package Description90 TABLET in 1 BOTTLE (69097-458-05)
Product NDC69097-458
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20161215
Marketing Category NameANDA
Application NumberANDA208709
ManufacturerCipla USA Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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