COZAAR - 0006-0952-31 - (losartan potassium)

Alphabetical Index


Drug Information of COZAAR

Product NDC: 0006-0952
Proprietary Name: COZAAR
Non Proprietary Name: losartan potassium
Active Ingredient(s): 50    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: 0006-0952
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020386
Marketing Category: NDA
Start Marketing Date: 19950414

Package Information of COZAAR

Package NDC: 0006-0952-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0006-0952-31)

NDC Information of COZAAR

NDC Code 0006-0952-31
Proprietary Name COZAAR
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0006-0952-31)
Product NDC 0006-0952
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950414
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name LOSARTAN POTASSIUM
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of COZAAR


General Information