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"68084-835-32" National Drug Code (NDC)

Fenofibrate 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-835-32) > 1 CAPSULE in 1 BLISTER PACK (68084-835-33)
(American Health Packaging)

NDC Code68084-835-32
Package Description20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-835-32) > 1 CAPSULE in 1 BLISTER PACK (68084-835-33)
Product NDC68084-835
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20140923
End Marketing Date20230131
Marketing Category NameANDA
Application NumberANDA075868
ManufacturerAmerican Health Packaging
Substance NameFENOFIBRATE
Strength134
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-835-32





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