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"70518-4721-0" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4721-0)
(REMEDYREPACK INC.)

NDC Code70518-4721-0
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4721-0)
Product NDC70518-4721
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260804
Marketing Category NameANDA
Application NumberANDA216798
ManufacturerREMEDYREPACK INC.
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/70518-4721-0





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