HYZAAR - 0006-0745-54 - (losartan potassium and hydrochlorothiazide)

Alphabetical Index


Drug Information of HYZAAR

Product NDC: 0006-0745
Proprietary Name: HYZAAR
Non Proprietary Name: losartan potassium and hydrochlorothiazide
Active Ingredient(s): 12.5; 100    mg/1; mg/1 & nbsp;   losartan potassium and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of HYZAAR

Product NDC: 0006-0745
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020387
Marketing Category: NDA
Start Marketing Date: 19950428

Package Information of HYZAAR

Package NDC: 0006-0745-54
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0006-0745-54)

NDC Information of HYZAAR

NDC Code 0006-0745-54
Proprietary Name HYZAAR
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0006-0745-54)
Product NDC 0006-0745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name losartan potassium and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950428
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of HYZAAR


General Information