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"71205-366-90" National Drug Code (NDC)
Fenofibrate 90 TABLET in 1 BOTTLE (71205-366-90)
(Proficient Rx LP)
NDC Code
71205-366-90
Package Description
90 TABLET in 1 BOTTLE (71205-366-90)
Product NDC
71205-366
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20151123
Marketing Category Name
ANDA
Application Number
ANDA204019
Manufacturer
Proficient Rx LP
Substance Name
FENOFIBRATE
Strength
54
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-366-90