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"68788-7579-6" National Drug Code (NDC)
Fenofibrate 60 TABLET in 1 BOTTLE (68788-7579-6)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-7579-6
Package Description
60 TABLET in 1 BOTTLE (68788-7579-6)
Product NDC
68788-7579
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20161215
Marketing Category Name
ANDA
Application Number
ANDA208709
Manufacturer
Preferred Pharmaceuticals, Inc.
Substance Name
FENOFIBRATE
Strength
145
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68788-7579-6