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"42385-935-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (42385-935-30)
(Laurus Labs Limited)

NDC Code42385-935-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (42385-935-30)
Product NDC42385-935
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200113
Marketing Category NameANDA
Application NumberANDA210606
ManufacturerLaurus Labs Limited
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42385-935-30





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