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"71335-1701-2" National Drug Code (NDC)
Fenofibrate 90 TABLET, COATED in 1 BOTTLE (71335-1701-2)
(Bryant Ranch Prepack)
NDC Code
71335-1701-2
Package Description
90 TABLET, COATED in 1 BOTTLE (71335-1701-2)
Product NDC
71335-1701
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20160505
Marketing Category Name
ANDA
Application Number
ANDA205118
Manufacturer
Bryant Ranch Prepack
Substance Name
FENOFIBRATE
Strength
48
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1701-2