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"42043-171-09" National Drug Code (NDC)
Fenofibrate 90 TABLET, COATED in 1 BOTTLE (42043-171-09)
(Karalex Pharma LLC)
NDC Code
42043-171-09
Package Description
90 TABLET, COATED in 1 BOTTLE (42043-171-09)
Product NDC
42043-171
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20091120
Marketing Category Name
ANDA
Application Number
ANDA076520
Manufacturer
Karalex Pharma LLC
Substance Name
FENOFIBRATE
Strength
160
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42043-171-09