www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"71335-0872-1" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (71335-0872-1)
(Bryant Ranch Prepack)

NDC Code71335-0872-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-0872-1)
Product NDC71335-0872
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180601
Marketing Category NameANDA
Application NumberANDA200884
ManufacturerBryant Ranch Prepack
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0872-1





Copyright © 2007-2024 www.ndcvalidator.com