MedPath

MANNITOL INJECTION, USP

MANNITOL INJECTION, USP

Approved
DIN Number

02243176

Drug Class

Human

Market Date

Apr 9, 2002

Company
HC

fresenius kabi canada ltd

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 Number02243176
AIG Number0103277001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Ethical
A
ATC Code
B05BC01 MANNITOL
Product Specifications
Dosage FormSolution
Route of AdministrationIntravenous
AHFS Classification40:28.12
Health Canada Classification

ACTIVE INGREDIENTS (1)

MANNITOLActive
Strength: 25 %
Monograph: MANNITOL

MedPath

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

© 2025 MedPath, Inc. All rights reserved.