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"69315-290-05" National Drug Code (NDC)
Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
(Leading Pharma, LLC)
NDC Code
69315-290-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
Product NDC
69315-290
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220820
Marketing Category Name
ANDA
Application Number
ANDA210606
Manufacturer
Leading Pharma, LLC
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/69315-290-05