"71610-027-83" National Drug Code (NDC)

Fenofibrate 3600 TABLET in 1 BOTTLE (71610-027-83)
(Aphena Pharma Solutions - Tennessee, LLC)

NDC Code71610-027-83
Package Description3600 TABLET in 1 BOTTLE (71610-027-83)
Product NDC71610-027
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20140813
Marketing Category NameANDA
Application NumberANDA090715
ManufacturerAphena Pharma Solutions - Tennessee, LLC
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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