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"70934-567-30" National Drug Code (NDC)
Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-567-30)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)
NDC Code
70934-567-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-567-30)
Product NDC
70934-567
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200227
Marketing Category Name
ANDA
Application Number
ANDA204598
Manufacturer
Denton Pharma, Inc. dba Northwind Pharmaceuticals
Substance Name
FENOFIBRATE
Strength
48
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70934-567-30