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"21695-732-90" National Drug Code (NDC)
Gemfibrozil 90 TABLET, FILM COATED in 1 BOTTLE (21695-732-90)
(Rebel Distributors Corp)
NDC Code
21695-732-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (21695-732-90)
Product NDC
21695-732
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemfibrozil
Non-Proprietary Name
Gemfibrozil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20101109
Marketing Category Name
ANDA
Application Number
ANDA077836
Manufacturer
Rebel Distributors Corp
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/21695-732-90