"42858-660-45" National Drug Code (NDC)

NDC Code	42858-660-45
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (42858-660-45)
Product NDC	42858-660
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fenofibrate
Non-Proprietary Name	Fenofibrate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20170601
Marketing Category Name	ANDA
Application Number	ANDA076433
Manufacturer	Rhodes Pharmaceuticals L.P.
Substance Name	FENOFIBRATE
Strength	160
Strength Unit	mg/1
Pharmacy Classes	Peroxisome Proliferator Receptor alpha Agonist [EPC]