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"82619-101-01" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (82619-101-01)
(Creekwood Pharmaceuticals LLC)

NDC Code82619-101-01
Package Description90 TABLET in 1 BOTTLE (82619-101-01)
Product NDC82619-101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230907
Marketing Category NameANDA
Application NumberANDA217732
ManufacturerCreekwood Pharmaceuticals LLC
Substance NameFENOFIBRATE
Strength40
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/82619-101-01





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