"60760-901-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-901-30)
(St Marys Medical Park Pharmacy)

NDC Code60760-901-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-901-30)
Product NDC60760-901
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100201
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerSt Marys Medical Park Pharmacy
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

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