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"72603-841-02" National Drug Code (NDC)

Fenofibrate 500 TABLET in 1 BOTTLE (72603-841-02)
(NorthStar RxLLC)

NDC Code72603-841-02
Package Description500 TABLET in 1 BOTTLE (72603-841-02)
Product NDC72603-841
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20250929
Marketing Category NameANDA
Application NumberANDA213864
ManufacturerNorthStar RxLLC
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/72603-841-02





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