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"68071-2135-3" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (68071-2135-3)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-2135-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-2135-3)
Product NDC68071-2135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060510
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-2135-3





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