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"70518-3370-0" National Drug Code (NDC)

Fenofibrate 30 POUCH in 1 BOX (70518-3370-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3370-1)
(REMEDYREPACK INC.)

NDC Code70518-3370-0
Package Description30 POUCH in 1 BOX (70518-3370-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3370-1)
Product NDC70518-3370
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220223
Marketing Category NameANDA
Application NumberANDA210670
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/70518-3370-0





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