Product information
From Health Canada
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:
2009-09-28
Original market date: See footnote 1
2009-09-28
Product name:
MULTAQ
Description:
FILM-COATED TABLETS
DIN:
02330989
Product Monograph/Veterinary Labelling:
Date:
2024-10-01
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
SANOFI-AVENTIS CANADA INC
1755 Steeles Avenue West
Toronto
Ontario
Canada
M2R 3T4
Class:
Human
Dosage form(s):
Tablet
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
24:04.04.20
Anatomical Therapeutic Chemical (ATC): See footnote 4
C01BD07 DRONEDARONE
Active ingredient group (AIG) number:See footnote5
0152642001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| DRONEDARONE (DRONEDARONE HYDROCHLORIDE) | 400 MG |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
| Additional Risk Minimization Measures |
|---|
| Healthcare Professional Education |