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Valsartan and Hydrochlorothiazide - 0781-5952-37 - (valsartan and hydrochlorothiazide)

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Drug Information of Valsartan and Hydrochlorothiazide

Product NDC: 0781-5952
Proprietary Name: Valsartan and Hydrochlorothiazide
Non Proprietary Name: valsartan and hydrochlorothiazide
Active Ingredient(s): 25; 320    mg/1; mg/1 & nbsp;   valsartan and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Valsartan and Hydrochlorothiazide

Product NDC: 0781-5952
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020818
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120921

Package Information of Valsartan and Hydrochlorothiazide

Package NDC: 0781-5952-37
Package Description: 3500 TABLET, FILM COATED in 1 BOTTLE (0781-5952-37)

NDC Information of Valsartan and Hydrochlorothiazide

NDC Code 0781-5952-37
Proprietary Name Valsartan and Hydrochlorothiazide
Package Description 3500 TABLET, FILM COATED in 1 BOTTLE (0781-5952-37)
Product NDC 0781-5952
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valsartan and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 25; 320
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 Valsartan and Hydrochlorothiazide


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