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"62135-837-90" National Drug Code (NDC)
Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (62135-837-90)
(Chartwell RX, LLC)
NDC Code
62135-837-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-837-90)
Product NDC
62135-837
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190211
Marketing Category Name
ANDA
Application Number
ANDA209660
Manufacturer
Chartwell RX, LLC
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/62135-837-90