"60505-3120-1" National Drug Code (NDC)

Fenofibrate 100 CAPSULE in 1 BOTTLE (60505-3120-1)
(Apotex Corp.)

NDC Code60505-3120-1
Package Description100 CAPSULE in 1 BOTTLE (60505-3120-1)
Product NDC60505-3120
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20130726
Marketing Category NameANDA
Application NumberANDA202252
ManufacturerApotex Corp.
Substance NameFENOFIBRATE
Strength43
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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