"27241-117-05" National Drug Code (NDC)

Fenofibrate 500 TABLET in 1 BOTTLE (27241-117-05)
(Ajanta Pharma USA Inc.)

NDC Code27241-117-05
Package Description500 TABLET in 1 BOTTLE (27241-117-05)
Product NDC27241-117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180720
Marketing Category NameANDA
Application NumberANDA210138
ManufacturerAjanta Pharma USA Inc.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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