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"68788-7662-9" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (68788-7662-9)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7662-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68788-7662-9)
Product NDC68788-7662
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200228
Marketing Category NameANDA
Application NumberANDA209660
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7662-9





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