"63304-444-05" National Drug Code (NDC)

Fenofibrate 500 CAPSULE in 1 BOTTLE (63304-444-05)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-444-05
Package Description500 CAPSULE in 1 BOTTLE (63304-444-05)
Product NDC63304-444
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20150302
Marketing Category NameANDA
Application NumberANDA201748
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameFENOFIBRATE
Strength130
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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