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"61919-831-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (61919-831-30)
(DirectRX)

NDC Code61919-831-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-831-30)
Product NDC61919-831
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerDirectRX
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-831-30





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