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Valsartan and Hydrochlorothiazide - 0378-6321-77 - (valsartan and hydrochlorothiazide)

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Drug Information of Valsartan and Hydrochlorothiazide

Product NDC: 0378-6321
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: 0378-6321
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078020
Marketing Category: ANDA
Start Marketing Date: 20120921

Package Information of Valsartan and Hydrochlorothiazide

Package NDC: 0378-6321-77
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6321-77)

NDC Information of Valsartan and Hydrochlorothiazide

NDC Code 0378-6321-77
Proprietary Name Valsartan and Hydrochlorothiazide
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6321-77)
Product NDC 0378-6321
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 ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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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