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"35356-916-90" National Drug Code (NDC)
Fenofibrate 90 TABLET in 1 BOTTLE (35356-916-90)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
35356-916-90
Package Description
90 TABLET in 1 BOTTLE (35356-916-90)
Product NDC
35356-916
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fenofibrate
Non-Proprietary Name
Fenofibrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100201
Marketing Category Name
ANDA
Application Number
ANDA076509
Manufacturer
Lake Erie Medical DBA Quality Care Products LLC
Substance Name
FENOFIBRATE
Strength
160
Strength Unit
mg/1
Pharmacy Classes
Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/35356-916-90