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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

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section .

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  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

08:18.08.04   HIV FUSION INHIBITORS

Anatomical Therapeutic Chemical (ATC): See footnote 4

J05AX07  ENFUVIRTIDE

Active ingredient group (AIG) number:See footnote 5

0149321001

List of active ingredient(s)
Active ingredient(s) Strength
ENFUVIRTIDE 108 MG / VIAL

Application information

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