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"0115-1522-10" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (0115-1522-10)
(Amneal Pharmaceuticals of New York LLC)

NDC Code0115-1522-10
Package Description90 TABLET in 1 BOTTLE (0115-1522-10)
Product NDC0115-1522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20150624
End Marketing Date20250831
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022118
ManufacturerAmneal Pharmaceuticals of New York LLC
Substance NameFENOFIBRATE
Strength40
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0115-1522-10





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