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Gemfibrozil - 21695-732-90 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 21695-732
Proprietary Name: Gemfibrozil
Non Proprietary Name: Gemfibrozil
Active Ingredient(s): 600    mg/1 & nbsp;   Gemfibrozil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Gemfibrozil

Product NDC: 21695-732
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077836
Marketing Category: ANDA
Start Marketing Date: 20101109

Package Information of Gemfibrozil

Package NDC: 21695-732-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (21695-732-90)

NDC Information of Gemfibrozil

NDC Code 21695-732-90
Proprietary Name Gemfibrozil
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (21695-732-90)
Product NDC 21695-732
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101109
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name GEMFIBROZIL
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Complete Information of Gemfibrozil


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