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"69367-257-09" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (69367-257-09)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-257-09
Package Description90 TABLET, FILM COATED in 1 BOTTLE (69367-257-09)
Product NDC69367-257
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200423
End Marketing Date20230131
Marketing Category NameANDA
Application NumberANDA207803
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69367-257-09





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