"60687-629-01" National Drug Code (NDC)

Fenofibrate 100 BLISTER PACK in 1 CARTON (60687-629-01) / 1 TABLET in 1 BLISTER PACK (60687-629-11)
(American Health Packaging)

NDC Code60687-629-01
Package Description100 BLISTER PACK in 1 CARTON (60687-629-01) / 1 TABLET in 1 BLISTER PACK (60687-629-11)
Product NDC60687-629
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20210624
Marketing Category NameANDA
Application NumberANDA090856
ManufacturerAmerican Health Packaging
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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