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:
2012-05-03
Original market date: See footnote 1
2008-07-12
Product name:
BENEFIX
Description:
ALSO KNOWN AS NONACOG ALFA
DIN:
02293803
Product Monograph/Veterinary Labelling:
Date:
2017-07-21
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
PFIZER CANADA ULC
17300 Trans-Canada Highway
Kirkland
Quebec
Canada
H9J 2M5
Class:
Human
Dosage form(s):
Powder For Solution
Route(s) of administration:
Intravenous
Number of active ingredient(s):
1
Schedule(s):
Schedule D
American Hospital Formulary Service (AHFS): See footnote 3
20:28.16
Anatomical Therapeutic Chemical (ATC): See footnote 4
B02BD04 COAGULATION FACTOR IX
Active ingredient group (AIG) number:See footnote5
0152202004
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| COAGULATION FACTOR IX (RECOMBINANT) | 2000 UNIT / VIAL |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.