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"51655-866-52" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE, PLASTIC (51655-866-52)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-866-52
Package Description30 TABLET in 1 BOTTLE, PLASTIC (51655-866-52)
Product NDC51655-866
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230710
Marketing Category NameANDA
Application NumberANDA208709
ManufacturerNorthwind Pharmaceuticals, LLC
Substance NameFENOFIBRATE
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51655-866-52





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