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"72789-410-30" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE, PLASTIC (72789-410-30)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-410-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (72789-410-30)
Product NDC72789-410
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20220622
Marketing Category NameANDA
Application NumberANDA076509
ManufacturerPD-Rx Pharmaceuticals, Inc.
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/72789-410-30





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