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"42043-170-09" National Drug Code (NDC)

Fenofibrate 90 TABLET, COATED in 1 BOTTLE (42043-170-09)
(Karalex Pharma LLC)

NDC Code42043-170-09
Package Description90 TABLET, COATED in 1 BOTTLE (42043-170-09)
Product NDC42043-170
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20091120
Marketing Category NameANDA
Application NumberANDA076520
ManufacturerKaralex Pharma LLC
Substance NameFENOFIBRATE
Strength54
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/42043-170-09





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