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"43598-909-90" National Drug Code (NDC)
Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)
(Dr. Reddy's Laboratories Inc.)
NDC Code
43598-909-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)
Product NDC
43598-909
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200131
Marketing Category Name
ANDA
Application Number
ANDA210670
Manufacturer
Dr. Reddy's Laboratories Inc.
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/43598-909-90