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"68682-525-01" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (68682-525-01)
(Oceanside Pharmaceuticals)

NDC Code68682-525-01
Package Description90 TABLET in 1 BOTTLE (68682-525-01)
Product NDC68682-525
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20120625
End Marketing Date20150930
Marketing Category NameANDA
Application NumberANDA090715
ManufacturerOceanside Pharmaceuticals
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68682-525-01





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