"43975-306-50" National Drug Code (NDC)

Fenofibrate 500 CAPSULE in 1 BOTTLE (43975-306-50)
(ANI Pharmaceuticals, Inc.)

NDC Code43975-306-50
Package Description500 CAPSULE in 1 BOTTLE (43975-306-50)
Product NDC43975-306
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20180501
Marketing Category NameANDA
Application NumberANDA209504
ManufacturerANI Pharmaceuticals, Inc.
Substance NameFENOFIBRATE
Strength200
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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