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"46708-350-71" National Drug Code (NDC)
Fenofibrate 500 TABLET, FILM COATED in 1 BOTTLE (46708-350-71)
(Alembic Pharmaceuticals Limited)
NDC Code
46708-350-71
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (46708-350-71)
Product NDC
46708-350
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200123
Marketing Category Name
ANDA
Application Number
ANDA213252
Manufacturer
Alembic Pharmaceuticals Limited
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/46708-350-71