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The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2015-11-25

Original market date: See footnote 1

2004-07-06

Product name:

TEVETEN PLUS

Description:

FILM-COATED TABLETS

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section .

DIN:

02253631

Product Monograph/Veterinary Labelling:

Date: 2021-02-24 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

BGP PHARMA ULC
85 Advance Road
Etobicoke
Ontario
Canada  M8Z 2S6

Class: 

Human

Dosage form(s):

Tablet

Route(s) of administration:

Oral

Number of active ingredient(s):

2

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

40:28.20   THIAZIDE DIURETICS ,  24:32.08   ANGIOTENSIN II RECEPTOR ANTAGONISTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

C09DA02  EPROSARTAN AND DIURETICS

Active ingredient group (AIG) number:See footnote 5

0250121001

List of active ingredient(s)
Active ingredient(s) Strength
EPROSARTAN (EPROSARTAN MESYLATE) 600 MG
HYDROCHLOROTHIAZIDE 12.5 MG

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