Product information
From Health Canada
No match found
No other product was found with the same active ingredient group.
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:
2003-08-18
Original market date: See footnote 1
2003-08-18
Product name:
FUZEON
Description:
SINGLE USE VIAL
DIN:
02247725
Product Monograph/Veterinary Labelling:
Date:
2020-03-25
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
HOFFMANN-LA ROCHE LIMITED
7070 Mississauga Road
Mississauga
Ontario
Canada
L5N 5M8
Class:
Human
Dosage form(s):
Powder For Solution
Route(s) of administration:
Subcutaneous
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
08:18.08.04
Anatomical Therapeutic Chemical (ATC): See footnote 4
J05AX07 ENFUVIRTIDE
Active ingredient group (AIG) number:See footnote5
0149321001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| ENFUVIRTIDE | 108 MG / VIAL |