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"59651-576-90" National Drug Code (NDC)
Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (59651-576-90)
(Aurobindo Pharma Limited)
NDC Code
59651-576-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (59651-576-90)
Product NDC
59651-576
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220927
Marketing Category Name
ANDA
Application Number
ANDA216798
Manufacturer
Aurobindo Pharma Limited
Substance Name
FENOFIBRATE
Strength
160
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59651-576-90