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"51655-901-52" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-901-52)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-901-52
Package Description30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-901-52)
Product NDC51655-901
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150224
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerNorthwind Pharmaceuticals, LLC
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/51655-901-52





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