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"71205-169-90" National Drug Code (NDC)
Gemfibrozil 90 TABLET, FILM COATED in 1 BOTTLE (71205-169-90)
(Proficient Rx LP)
NDC Code
71205-169-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (71205-169-90)
Product NDC
71205-169
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150916
Marketing Category Name
ANDA
Application Number
ANDA202726
Manufacturer
Proficient Rx LP
Substance Name
GEMFIBROZIL
Strength
600
Strength Unit
mg/1
Pharmacy Classes
PPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-169-90