www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"63304-900-10" National Drug Code (NDC)
Fenofibrate 1000 TABLET, FILM COATED in 1 BOTTLE (63304-900-10)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
63304-900-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (63304-900-10)
Product NDC
63304-900
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200918
Marketing Category Name
ANDA
Application Number
ANDA076635
Manufacturer
Sun Pharmaceutical Industries, 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/63304-900-10