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Gemfibrozil - 49349-389-02 - (Gemfibrozil)

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Drug Information of Gemfibrozil

Product NDC: 49349-389
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: 49349-389
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077836
Marketing Category: ANDA
Start Marketing Date: 20110719

Package Information of Gemfibrozil

Package NDC: 49349-389-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-389-02)

NDC Information of Gemfibrozil

NDC Code 49349-389-02
Proprietary Name Gemfibrozil
Package Description 30 TABLET in 1 BLISTER PACK (49349-389-02)
Product NDC 49349-389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemfibrozil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110719
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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