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Valsartan and Hydrochlorothiazide - 68180-101-02 - (Valsartan and Hydrochlorothiazide)

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Drug Information of Valsartan and Hydrochlorothiazide

Product NDC: 68180-101
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: 68180-101
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078946
Marketing Category: ANDA
Start Marketing Date: 20130321

Package Information of Valsartan and Hydrochlorothiazide

Package NDC: 68180-101-02
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (68180-101-02)

NDC Information of Valsartan and Hydrochlorothiazide

NDC Code 68180-101-02
Proprietary Name Valsartan and Hydrochlorothiazide
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (68180-101-02)
Product NDC 68180-101
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 Lupin Pharmaceuticals, Inc.
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 12.5; 320
Strength Unit mg/1; mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Valsartan and Hydrochlorothiazide


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