ARZERRA
ARZERRA
Discontinued
DIN Number
02381567
Drug Class
Human
Market Date
Aug 13, 2012
Company
HC
novartis pharmaceuticals 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 Number02381567
AIG Number0153129001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D
,
Prescription
A
ATC Code
L01FA02 OFATUMUMAB
Product Specifications
Dosage FormSolution
Route of AdministrationIntravenous
AHFS Classification10:00.00
Health Canada Classification
ACTIVE INGREDIENTS (1)
OFATUMUMABActive
Strength: 1000 MG / 50 ML
Monograph: OFATUMUMAB