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"71335-1211-1" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (71335-1211-1)
(Bryant Ranch Prepack)

NDC Code71335-1211-1
Package Description30 TABLET in 1 BOTTLE (71335-1211-1)
Product NDC71335-1211
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20161215
Marketing Category NameANDA
Application NumberANDA208709
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1211-1





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