MedPath

XYNTHA SOLOFUSE

XYNTHA SOLOFUSE

Approved
DIN Number

02374099

Drug Class

Human

Market Date

May 8, 2012

Company
HC

Pfizer Canada Ulc

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 Number02374099
AIG Number0147521005
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D
A
ATC Code
B02BD02 COAGULATION FACTOR VIII
Product Specifications
Dosage FormPowder For Solution
Route of AdministrationIntravenous
AHFS Classification20:28.16
Health Canada Classification

ACTIVE INGREDIENTS (1)

MOROCTOCOG ALFAActive
Strength: 3000 UNIT / SYR
Monograph: MOROCTOCOG ALFA

MedPath

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

© 2025 MedPath, Inc. All rights reserved.