"58118-5522-8" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BLISTER PACK (58118-5522-8)
(Clinical Solutions Wholesale)

NDC Code58118-5522-8
Package Description30 TABLET in 1 BLISTER PACK (58118-5522-8)
Product NDC58118-5522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerClinical Solutions Wholesale
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

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