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"0615-3559-39" National Drug Code (NDC)
Gemfibrozil 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)
NDC Code
0615-3559-39
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3559-39)
Product NDC
0615-3559
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19931124
Marketing Category Name
ANDA
Application Number
ANDA074256
Manufacturer
NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name
GEMFIBROZIL
Strength
600
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/0615-3559-39