"68084-329-21" National Drug Code (NDC)

Fenofibrate 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-329-21) > 1 CAPSULE in 1 BLISTER PACK (68084-329-11)
(American Health Packaging)

NDC Code68084-329-21
Package Description30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-329-21) > 1 CAPSULE in 1 BLISTER PACK (68084-329-11)
Product NDC68084-329
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20090121
End Marketing Date20230731
Marketing Category NameANDA
Application NumberANDA075868
ManufacturerAmerican Health Packaging
Substance NameFENOFIBRATE
Strength200
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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