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"35561-343-13" National Drug Code (NDC)
Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13)
(AustarPharma LLC)
NDC Code
35561-343-13
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (35561-343-13)
Product NDC
35561-343
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190630
Marketing Category Name
ANDA
Application Number
ANDA207803
Manufacturer
AustarPharma 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/35561-343-13