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"63629-7151-1" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (63629-7151-1)
(Bryant Ranch Prepack)

NDC Code63629-7151-1
Package Description30 TABLET in 1 BOTTLE (63629-7151-1)
Product NDC63629-7151
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63629-7151-1





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