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:
2019-10-29
Original market date: See footnote 1
2019-10-29
Product name:
RADICAVA
DIN:
02475472
Product Monograph/Veterinary Labelling:
Date:
2022-11-08
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
MITSUBISHI TANABE PHARMA CORPORATION
3-2-10 Doshomachi
Chuo-Ku
Osaka-Fu
Japan
541-0045
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Intravenous
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
28:92.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
N07XX14 EDARAVONE
Active ingredient group (AIG) number:See footnote5
0160190001
| Active ingredient(s) | Strength |
|---|---|
| EDARAVONE | 30 MG / 100 ML |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
| Pharmacovigilance/Monitoring Activity |
|---|
| Drug Utilisation Study (DUS) |