MedPath

TZIELD

TZIELD

Approved
DIN Number

02557347

Drug Class

Human

Market Date

N/A

Company
HC

sanofi-aventis canada inc

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 Number02557347
AIG Number0166824001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D ,  Prescription
A
ATC Code
A10XX01 TEPLIZUMAB
Product Specifications
Dosage FormSolution
Route of AdministrationIntravenous
AHFS Classification68:20.92
Health Canada Classification

ACTIVE INGREDIENTS (1)

TEPLIZUMABActive
Strength: 2 MG / 2 ML
Monograph: TEPLIZUMAB

MedPath

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

© 2025 MedPath, Inc. All rights reserved.