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"27241-117-03" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (27241-117-03)
(Ajanta Pharma USA Inc.)

NDC Code27241-117-03
Package Description90 TABLET in 1 BOTTLE (27241-117-03)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/27241-117-03





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