"69315-290-05" National Drug Code (NDC)

Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
(Leading Pharma, LLC)

NDC Code69315-290-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
Product NDC69315-290
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220820
Marketing Category NameANDA
Application NumberANDA210606
ManufacturerLeading Pharma, LLC
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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