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Valsartan and Hydrochlorothiazide - 33342-077-15 - (Valsartan and Hydrochlorothiazide)

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Drug Information of Valsartan and Hydrochlorothiazide

Product NDC: 33342-077
Proprietary Name: Valsartan and Hydrochlorothiazide
Non Proprietary Name: Valsartan and Hydrochlorothiazide
Active Ingredient(s): 12.5; 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: 33342-077
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203145
Marketing Category: ANDA
Start Marketing Date: 20130419

Package Information of Valsartan and Hydrochlorothiazide

Package NDC: 33342-077-15
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (33342-077-15)

NDC Information of Valsartan and Hydrochlorothiazide

NDC Code 33342-077-15
Proprietary Name Valsartan and Hydrochlorothiazide
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (33342-077-15)
Product NDC 33342-077
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valsartan and Hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130419
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 12.5; 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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