"42385-951-90" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (42385-951-90)
(Laurus Labs Limited)

NDC Code42385-951-90
Package Description90 TABLET in 1 BOTTLE (42385-951-90)
Product NDC42385-951
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200318
Marketing Category NameANDA
Application NumberANDA211122
ManufacturerLaurus Labs Limited
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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