MedPath

COLUMVI

COLUMVI

Approved
DIN Number

02536552

Drug Class

Human

Market Date

Jul 5, 2023

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 Number02536552
AIG Number0164522001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription ,  Schedule D
A
ATC Code
L01FX28 GLOFITAMAB
Product Specifications
Dosage FormSolution
Route of AdministrationIntravenous
AHFS Classification10:00.00
Health Canada Classification

ACTIVE INGREDIENTS (1)

GLOFITAMABActive
Strength: 2.5 MG / 2.5 ML
Monograph: GLOFITAMAB

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