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"63304-449-05" National Drug Code (NDC)

Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-449-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)
Product NDC63304-449
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180601
Marketing Category NameANDA
Application NumberANDA200884
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63304-449-05





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