"46708-555-90" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (46708-555-90)
(Alembic Pharmaceuticals Limited)

NDC Code46708-555-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (46708-555-90)
Product NDC46708-555
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190801
Marketing Category NameANDA
Application NumberANDA209660
ManufacturerAlembic Pharmaceuticals Limited
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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