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"68788-7579-3" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (68788-7579-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7579-3
Package Description30 TABLET in 1 BOTTLE (68788-7579-3)
Product NDC68788-7579
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20161215
Marketing Category NameANDA
Application NumberANDA208709
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7579-3





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