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"72162-2170-9" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (72162-2170-9)
(Bryant Ranch Prepack)

NDC Code72162-2170-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (72162-2170-9)
Product NDC72162-2170
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200131
Marketing Category NameANDA
Application NumberANDA210670
ManufacturerBryant Ranch Prepack
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/72162-2170-9





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