"49349-157-02" National Drug Code (NDC)

Fenofibrate 30 CAPSULE in 1 BLISTER PACK (49349-157-02)
(REMEDYREPACK INC.)

NDC Code49349-157-02
Package Description30 CAPSULE in 1 BLISTER PACK (49349-157-02)
Product NDC49349-157
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20110413
Marketing Category NameANDA
Application NumberANDA075868
ManufacturerREMEDYREPACK INC.
Substance NameFENOFIBRATE
Strength134
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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