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"70756-215-51" National Drug Code (NDC)

Fenofibrate 500 TABLET in 1 BOTTLE (70756-215-51)
(Lifestar Pharma LLC)

NDC Code70756-215-51
Package Description500 TABLET in 1 BOTTLE (70756-215-51)
Product NDC70756-215
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200910
Marketing Category NameANDA
Application NumberANDA213864
ManufacturerLifestar Pharma LLC
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/70756-215-51





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