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:
2020-03-12
Original market date: See footnote 1
2015-04-28
Product name:
FERRIPROX
DIN:
02436558
Product Monograph/Veterinary Labelling:
Date:
2023-03-29
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
CHIESI CANADA CORP.
100e-3800 Steeles Avenue West
Woodbridge
Ontario
Canada
L4L 4G9
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
64:00.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
V03AC02 DEFERIPRONE
Active ingredient group (AIG) number:See footnote5
0156430003
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| DEFERIPRONE | 1000 MG |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
| Additional Risk Minimization Measures |
|---|
| Controlled Distribution Program |
| Patient Education |
| Healthcare Professional Education |
| Patient Wallet Card |