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"70518-2349-0" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE, PLASTIC (70518-2349-0)
(REMEDYREPACK INC.)

NDC Code70518-2349-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-2349-0)
Product NDC70518-2349
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20191006
Marketing Category NameANDA
Application NumberANDA210138
ManufacturerREMEDYREPACK INC.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2349-0





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