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"16714-740-01" National Drug Code (NDC)
Fenofibrate 90 CAPSULE in 1 BOTTLE, PLASTIC (16714-740-01)
(Northstar Rx LLC)
NDC Code
16714-740-01
Package Description
90 CAPSULE in 1 BOTTLE, PLASTIC (16714-740-01)
Product NDC
16714-740
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20170821
Marketing Category Name
ANDA
Application Number
ANDA207378
Manufacturer
Northstar Rx LLC
Substance Name
FENOFIBRATE
Strength
134
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-740-01