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"33342-339-10" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (33342-339-10)
(Macleods Pharmaceuticals Limited)

NDC Code33342-339-10
Package Description90 TABLET in 1 BOTTLE (33342-339-10)
Product NDC33342-339
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20241113
Marketing Category NameANDA
Application NumberANDA210248
ManufacturerMacleods Pharmaceuticals Limited
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/33342-339-10





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