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"35561-249-13" National Drug Code (NDC)

Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (35561-249-13)
(AustarPharma, LLC)

NDC Code35561-249-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (35561-249-13)
Product NDC35561-249
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210101
Marketing Category NameANDA
Application NumberANDA208476
ManufacturerAustarPharma, 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/35561-249-13





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