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Valsartan and Hydrochlorothiazide - 65862-547-10 - (Valsartan and Hydrochlorothiazide)

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Drug Information of Valsartan and Hydrochlorothiazide

Product NDC: 65862-547
Proprietary Name: Valsartan and Hydrochlorothiazide
Non Proprietary Name: Valsartan and Hydrochlorothiazide
Active Ingredient(s): 12.5; 80    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: 65862-547
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202519
Marketing Category: ANDA
Start Marketing Date: 20130321

Package Information of Valsartan and Hydrochlorothiazide

Package NDC: 65862-547-10
Package Description: 10 BLISTER PACK in 1 CARTON (65862-547-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Valsartan and Hydrochlorothiazide

NDC Code 65862-547-10
Proprietary Name Valsartan and Hydrochlorothiazide
Package Description 10 BLISTER PACK in 1 CARTON (65862-547-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 65862-547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valsartan and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130321
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 12.5; 80
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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