"35356-603-90" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-603-90)
(Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC)

NDC Code35356-603-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-603-90)
Product NDC35356-603
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110113
Marketing Category NameANDA
Application NumberANDA076520
ManufacturerLake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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