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losartan potassium and hydrochlorothiazide - 0781-5818-31 - (losartan potassium and hydrochlorothiazide)

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Drug Information of losartan potassium and hydrochlorothiazide

Product NDC: 0781-5818
Proprietary Name: losartan potassium and hydrochlorothiazide
Non Proprietary Name: losartan potassium and hydrochlorothiazide
Active Ingredient(s): 25; 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 losartan potassium and hydrochlorothiazide

Product NDC: 0781-5818
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020387
Marketing Category: NDA
Start Marketing Date: 19950428

Package Information of losartan potassium and hydrochlorothiazide

Package NDC: 0781-5818-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-5818-31)

NDC Information of losartan potassium and hydrochlorothiazide

NDC Code 0781-5818-31
Proprietary Name losartan potassium and hydrochlorothiazide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0781-5818-31)
Product NDC 0781-5818
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 Sandoz Inc.
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 25; 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 losartan potassium and hydrochlorothiazide


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