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"71205-949-78" National Drug Code (NDC)
Fenofibrate 180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
(Proficient Rx LP)
NDC Code
71205-949-78
Package Description
180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
Product NDC
71205-949
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200423
Marketing Category Name
ANDA
Application Number
ANDA207803
Manufacturer
Proficient Rx LP
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/71205-949-78