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"50436-0172-1" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (50436-0172-1)
(Unit Dose Services)

NDC Code50436-0172-1
Package Description30 TABLET in 1 BOTTLE (50436-0172-1)
Product NDC50436-0172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerUnit Dose Services
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/50436-0172-1





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