Diovan HCT - 55289-820-30 - (valsartan and hydrochlorothiazide)

Alphabetical Index


Drug Information of Diovan HCT

Product NDC: 55289-820
Proprietary Name: Diovan HCT
Non Proprietary Name: valsartan and hydrochlorothiazide
Active Ingredient(s): 25; 160    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: 55289-820
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020818
Marketing Category: NDA
Start Marketing Date: 19980306

Package Information of Diovan HCT

Package NDC: 55289-820-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-820-30)

NDC Information of Diovan HCT

NDC Code 55289-820-30
Proprietary Name Diovan HCT
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-820-30)
Product NDC 55289-820
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name valsartan and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980306
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name HYDROCHLOROTHIAZIDE; VALSARTAN
Strength Number 25; 160
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 Diovan HCT


General Information