"82868-018-30" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE, PLASTIC (82868-018-30)
(Northwind Pharmaceuticals, LLC)

NDC Code82868-018-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (82868-018-30)
Product NDC82868-018
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20231017
Marketing Category NameANDA
Application NumberANDA090856
ManufacturerNorthwind Pharmaceuticals, LLC
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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