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"68071-2686-9" National Drug Code (NDC)
Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2686-9)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-2686-9
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2686-9)
Product NDC
68071-2686
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20130514
Marketing Category Name
ANDA
Application Number
ANDA202856
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/68071-2686-9