"50436-0171-1" National Drug Code (NDC)

Fenofibrate 30 CAPSULE in 1 BOTTLE (50436-0171-1)
(Unit Dose Services)

NDC Code50436-0171-1
Package Description30 CAPSULE in 1 BOTTLE (50436-0171-1)
Product NDC50436-0171
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA075868
ManufacturerUnit Dose Services
Substance NameFENOFIBRATE
Strength134
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

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