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Losartan potassium and hydrochlorothiazide - 0781-5206-01 - (Losartan potassium and hydrochlorothiazide tablets)

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Drug Information of Losartan potassium and hydrochlorothiazide

Product NDC: 0781-5206
Proprietary Name: Losartan potassium and hydrochlorothiazide
Non Proprietary Name: Losartan potassium and hydrochlorothiazide tablets
Active Ingredient(s): 12.5; 50    mg/1; mg/1 & nbsp;   Losartan potassium and hydrochlorothiazide tablets
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: 0781-5206
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077948
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Losartan potassium and hydrochlorothiazide

Package NDC: 0781-5206-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0781-5206-01)

NDC Information of Losartan potassium and hydrochlorothiazide

NDC Code 0781-5206-01
Proprietary Name Losartan potassium and hydrochlorothiazide
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0781-5206-01)
Product NDC 0781-5206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Losartan potassium and hydrochlorothiazide tablets
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101006
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength Number 12.5; 50
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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