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"27241-116-03" National Drug Code (NDC)
Fenofibrate 90 TABLET in 1 BOTTLE (27241-116-03)
(Ajanta Pharma USA Inc.)
NDC Code
27241-116-03
Package Description
90 TABLET in 1 BOTTLE (27241-116-03)
Product NDC
27241-116
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180720
Marketing Category Name
ANDA
Application Number
ANDA210138
Manufacturer
Ajanta Pharma USA 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/27241-116-03