"50742-202-01" National Drug Code (NDC)

Fenofibrate 100 CAPSULE in 1 BOTTLE (50742-202-01)
(Ingenus Pharmaceuticals, LLC)

NDC Code50742-202-01
Package Description100 CAPSULE in 1 BOTTLE (50742-202-01)
Product NDC50742-202
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20190425
Marketing Category NameANDA
Application NumberANDA207564
ManufacturerIngenus Pharmaceuticals, LLC
Substance NameFENOFIBRATE
Strength134
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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