"62332-555-91" National Drug Code (NDC)

Fenofibrate 1000 TABLET, FILM COATED in 1 BOTTLE (62332-555-91)
(Alembic Pharmaceuticals Inc.)

NDC Code62332-555-91
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (62332-555-91)
Product NDC62332-555
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 Inc.
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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