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"42385-950-90" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (42385-950-90)
(Laurus Labs Limited)

NDC Code42385-950-90
Package Description90 TABLET in 1 BOTTLE (42385-950-90)
Product NDC42385-950
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200318
Marketing Category NameANDA
Application NumberANDA211122
ManufacturerLaurus Labs 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/42385-950-90





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