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"69367-254-05" National Drug Code (NDC)

Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-254-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05)
Product NDC69367-254
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200423
Marketing Category NameANDA
Application NumberANDA207803
ManufacturerWestminster Pharmaceuticals, 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/69367-254-05





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