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"0115-1523-10" National Drug Code (NDC)
Fenofibrate 90 TABLET in 1 BOTTLE (0115-1523-10)
(Amneal Pharmaceuticals of New York LLC)
NDC Code
0115-1523-10
Package Description
90 TABLET in 1 BOTTLE (0115-1523-10)
Product NDC
0115-1523
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150624
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA022118
Manufacturer
Amneal Pharmaceuticals of New York LLC
Substance Name
FENOFIBRATE
Strength
120
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0115-1523-10