"83008-072-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (83008-072-30)
(Quality Care Products, LLC)

NDC Code83008-072-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (83008-072-30)
Product NDC83008-072
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240711
Marketing Category NameANDA
Application NumberANDA216798
ManufacturerQuality Care Products, LLC
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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