Lopid - 0071-0737-30 - (gemfibrozil)

Alphabetical Index


Drug Information of Lopid

Product NDC: 0071-0737
Proprietary Name: Lopid
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 Lopid

Product NDC: 0071-0737
Labeler Name: Parke-Davis Div of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018422
Marketing Category: NDA
Start Marketing Date: 20040330

Package Information of Lopid

Package NDC: 0071-0737-30
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0071-0737-30)

NDC Information of Lopid

NDC Code 0071-0737-30
Proprietary Name Lopid
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0071-0737-30)
Product NDC 0071-0737
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gemfibrozil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040330
Marketing Category Name NDA
Labeler Name Parke-Davis Div of Pfizer 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 Lopid


General Information