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"50090-7208-0" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (50090-7208-0)
(A-S Medication Solutions)

NDC Code50090-7208-0
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50090-7208-0)
Product NDC50090-7208
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220927
Marketing Category NameANDA
Application NumberANDA216798
ManufacturerA-S Medication Solutions
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/50090-7208-0





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