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"61786-283-19" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (61786-283-19)
(REMEDYREPACK INC.)

NDC Code61786-283-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61786-283-19)
Product NDC61786-283
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150429
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerREMEDYREPACK INC.
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/61786-283-19





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