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"60219-5522-9" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (60219-5522-9)
(Amneal Pharmaceuticals NY LLC)

NDC Code60219-5522-9
Package Description90 TABLET in 1 BOTTLE (60219-5522-9)
Product NDC60219-5522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20220622
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerAmneal Pharmaceuticals NY LLC
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/60219-5522-9





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