"68788-4006-6" National Drug Code (NDC)

Fenofibrate 60 TABLET in 1 BOTTLE (68788-4006-6)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-4006-6
Package Description60 TABLET in 1 BOTTLE (68788-4006-6)
Product NDC68788-4006
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20250808
Marketing Category NameANDA
Application NumberANDA090856
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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