MedPath

FUZEON

FUZEON

Discontinued
DIN Number

02247725

Drug Class

Human

Market Date

Aug 18, 2003

Company
HC

Hoffmann-La Roche Limited

Product Information

Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.

Product Details

Health Canada regulatory and product classification information

Regulatory Identifiers
DIN Number02247725
AIG Number0149321001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
J05AX07 ENFUVIRTIDE
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationSubcutaneous
AHFS Classification08:18.08.04
Health Canada Classification

ACTIVE INGREDIENTS (1)

ENFUVIRTIDEActive
Strength: 108 MG / VIAL
Monograph: ENFUVIRTIDE

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.