Cozaar - 54868-2335-1 - (losartan potassium)

Alphabetical Index


Drug Information of Cozaar

Product NDC: 54868-2335
Proprietary Name: Cozaar
Non Proprietary Name: losartan potassium
Active Ingredient(s): 100    mg/1 & nbsp;   losartan potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cozaar

Product NDC: 54868-2335
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020386
Marketing Category: NDA
Start Marketing Date: 20030806

Package Information of Cozaar

Package NDC: 54868-2335-1
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2335-1)

NDC Information of Cozaar

NDC Code 54868-2335-1
Proprietary Name Cozaar
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2335-1)
Product NDC 54868-2335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030806
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name LOSARTAN POTASSIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Cozaar


General Information