Tribenzor - 65597-114-90 - (olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide)

Alphabetical Index


Drug Information of Tribenzor

Product NDC: 65597-114
Proprietary Name: Tribenzor
Non Proprietary Name: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Active Ingredient(s): 5; 12.5; 20    mg/1; mg/1; mg/1 & nbsp;   olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tribenzor

Product NDC: 65597-114
Labeler Name: Daiichi Sankyo, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA200175
Marketing Category: NDA
Start Marketing Date: 20100731

Package Information of Tribenzor

Package NDC: 65597-114-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (65597-114-90)

NDC Information of Tribenzor

NDC Code 65597-114-90
Proprietary Name Tribenzor
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (65597-114-90)
Product NDC 65597-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100731
Marketing Category Name NDA
Labeler Name Daiichi Sankyo, Inc.
Substance Name AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength Number 5; 12.5; 20
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Tribenzor


General Information