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"71205-666-90" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (71205-666-90)
(Proficient Rx LP)

NDC Code71205-666-90
Package Description90 TABLET in 1 BOTTLE (71205-666-90)
Product NDC71205-666
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200910
Marketing Category NameANDA
Application NumberANDA213864
ManufacturerProficient Rx LP
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-666-90





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