"69367-269-01" National Drug Code (NDC)

Fenofibrate 100 CAPSULE in 1 BOTTLE (69367-269-01)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-269-01
Package Description100 CAPSULE in 1 BOTTLE (69367-269-01)
Product NDC69367-269
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20201120
Marketing Category NameANDA
Application NumberANDA207805
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameFENOFIBRATE
Strength200
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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