"68788-7578-9" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (68788-7578-9)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7578-9
Package Description90 TABLET in 1 BOTTLE (68788-7578-9)
Product NDC68788-7578
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180720
Marketing Category NameANDA
Application NumberANDA210138
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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