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"68788-8106-1" National Drug Code (NDC)
Fenofibrate 100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-8106-1
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
Product NDC
68788-8106
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20211103
Marketing Category Name
ANDA
Application Number
ANDA204598
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/68788-8106-1