"0904-7128-04" National Drug Code (NDC)

Fenofibrate 30 BLISTER PACK in 1 CARTON (0904-7128-04) / 1 TABLET in 1 BLISTER PACK
(Major Pharmaceuticals)

NDC Code0904-7128-04
Package Description30 BLISTER PACK in 1 CARTON (0904-7128-04) / 1 TABLET in 1 BLISTER PACK
Product NDC0904-7128
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200701
Marketing Category NameANDA
Application NumberANDA204019
ManufacturerMajor Pharmaceuticals
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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