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"69097-458-02" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (69097-458-02)
(Cipla USA Inc.)

NDC Code69097-458-02
Package Description30 TABLET in 1 BOTTLE (69097-458-02)
Product NDC69097-458
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20161215
Marketing Category NameANDA
Application NumberANDA208709
ManufacturerCipla USA Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-458-02





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