MedPath

MOZOBIL

MOZOBIL

Approved
DIN Number

02377225

Drug Class

Human

Market Date

Mar 26, 2012

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 Number02377225
AIG Number0153050001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
L03AX16 PLERIXAFOR
Product Specifications
Dosage FormSolution
Route of AdministrationSubcutaneous
AHFS Classification20:16.00
Health Canada Classification

ACTIVE INGREDIENTS (1)

PLERIXAFORActive
Strength: 20 MG / ML
Monograph: PLERIXAFOR

MedPath

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

© 2025 MedPath, Inc. All rights reserved.