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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:

2001-08-28

Original market date: See footnote 1

1993-12-31

Product name:

PREVORA STAGE 1

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:

02046245

Product Monograph/Veterinary Labelling:

Date: 2017-08-17 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

CHX TECHNOLOGIES INC
SUITE 603  40 University Ave
Toronto
Ontario
Canada  M5J 1T1

Class: 

Human

Dosage form(s):

Solution,  Kit

Route(s) of administration:

Dental

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

34:00.00   DENTAL AGENTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

A01AB03  CHLORHEXIDINE

Active ingredient group (AIG) number:See footnote 5

0107805006

List of active ingredient(s)
Active ingredient(s) Strength
CHLORHEXIDINE ACETATE 10 %

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