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"68180-362-02" National Drug Code (NDC)

Fenofibrate 500 TABLET in 1 BOTTLE (68180-362-02)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-362-02
Package Description500 TABLET in 1 BOTTLE (68180-362-02)
Product NDC68180-362
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20151123
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA204019
ManufacturerLupin 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/68180-362-02





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