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Gemfibrozil - 66336-367-30 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 66336-367
Proprietary Name: Gemfibrozil
Non Proprietary Name: Gemfibrozil
Active Ingredient(s): 600    mg/1 & nbsp;   Gemfibrozil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gemfibrozil

Product NDC: 66336-367
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077836
Marketing Category: ANDA
Start Marketing Date: 20060727

Package Information of Gemfibrozil

Package NDC: 66336-367-30
Package Description: 30 TABLET in 1 BOTTLE (66336-367-30)

NDC Information of Gemfibrozil

NDC Code 66336-367-30
Proprietary Name Gemfibrozil
Package Description 30 TABLET in 1 BOTTLE (66336-367-30)
Product NDC 66336-367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060727
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
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


General Information