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"68071-4486-2" National Drug Code (NDC)
Fenofibrate 20 TABLET, COATED in 1 BOTTLE (68071-4486-2)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-4486-2
Package Description
20 TABLET, COATED in 1 BOTTLE (68071-4486-2)
Product NDC
68071-4486
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20160505
Marketing Category Name
ANDA
Application Number
ANDA205118
Manufacturer
NuCare 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/68071-4486-2