"46708-350-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (46708-350-30)
(Alembic Pharmaceuticals Limited)

NDC Code46708-350-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (46708-350-30)
Product NDC46708-350
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200123
Marketing Category NameANDA
Application NumberANDA213252
ManufacturerAlembic Pharmaceuticals Limited
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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