"69315-287-09" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (69315-287-09)
(Leading Pharma, LLC)

NDC Code69315-287-09
Package Description90 TABLET in 1 BOTTLE (69315-287-09)
Product NDC69315-287
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20220718
Marketing Category NameANDA
Application NumberANDA211122
ManufacturerLeading Pharma, LLC
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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