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"70786-5522-1" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (70786-5522-1)
(Unit Dose Services)

NDC Code70786-5522-1
Package Description30 TABLET in 1 BOTTLE (70786-5522-1)
Product NDC70786-5522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerUnit Dose Services
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70786-5522-1





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