"65862-769-01" National Drug Code (NDC)

Fenofibrate 100 TABLET, COATED in 1 BOTTLE (65862-769-01)
(Aurobindo Pharma Limited)

NDC Code65862-769-01
Package Description100 TABLET, COATED in 1 BOTTLE (65862-769-01)
Product NDC65862-769
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20160505
Marketing Category NameANDA
Application NumberANDA205118
ManufacturerAurobindo Pharma Limited
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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