"68788-8106-1" National Drug Code (NDC)

Fenofibrate 100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-8106-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
Product NDC68788-8106
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211103
Marketing Category NameANDA
Application NumberANDA204598
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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