Diovan HCT - 35356-293-90 - (valsartan and hydrochlorothiazide)

Alphabetical Index


Drug Information of Diovan HCT

Product NDC: 35356-293
Proprietary Name: Diovan HCT
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 Diovan HCT

Product NDC: 35356-293
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020818
Marketing Category: NDA
Start Marketing Date: 20120228

Package Information of Diovan HCT

Package NDC: 35356-293-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (35356-293-90)

NDC Information of Diovan HCT

NDC Code 35356-293-90
Proprietary Name Diovan HCT
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (35356-293-90)
Product NDC 35356-293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valsartan and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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 Diovan HCT


General Information