"35561-343-13" National Drug Code (NDC)

Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13)
(AustarPharma LLC)

NDC Code35561-343-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13)
Product NDC35561-343
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190630
Marketing Category NameANDA
Application NumberANDA207803
ManufacturerAustarPharma LLC
Substance NameFENOFIBRATE
Strength54
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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