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"72189-172-30" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (72189-172-30)
(Direct_Rx)

NDC Code72189-172-30
Package Description30 TABLET in 1 BOTTLE (72189-172-30)
Product NDC72189-172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20210209
Marketing Category NameANDA
Application NumberANDA210138
ManufacturerDirect_Rx
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/72189-172-30





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