Home > National Drug Code (NDC) > Gemfibrozil

Gemfibrozil - 54868-2353-3 - (Gemfibrozil)

Alphabetical Index


Drug Information of Gemfibrozil

Product NDC: 54868-2353
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: 54868-2353
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074256
Marketing Category: ANDA
Start Marketing Date: 20040810

Package Information of Gemfibrozil

Package NDC: 54868-2353-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-2353-3)

NDC Information of Gemfibrozil

NDC Code 54868-2353-3
Proprietary Name Gemfibrozil
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-2353-3)
Product NDC 54868-2353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040810
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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