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"63304-901-03" National Drug Code (NDC)

Fenofibrate 10 TABLET, FILM COATED in 1 BOTTLE (63304-901-03)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-901-03
Package Description10 TABLET, FILM COATED in 1 BOTTLE (63304-901-03)
Product NDC63304-901
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200918
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerSun Pharmaceutical Industries, 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/63304-901-03





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