MedPath

ACTIFED DM TABLETS

ACTIFED DM TABLETS

Discontinued
DIN Number

02049821

Drug Class

Human

Market Date

Dec 31, 1994

Company
HC

glaxo wellcome 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 Number02049821
AIG Number0314239002
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
R05DA20 COMBINATIONS
Product Specifications
Dosage FormTablet
Route of AdministrationOral
AHFS Classification04:04.20
Health Canada Classification

ACTIVE INGREDIENTS (3)

DEXTROMETHORPHAN HYDROBROMIDEActive
Strength: 30 MG / TAB
Monograph: DEXTROMETHORPHAN HYDROBROMIDE
PSEUDOEPHEDRINE HYDROCHLORIDEActive
Strength: 60 MG / TAB
Monograph: PSEUDOEPHEDRINE HYDROCHLORIDE
TRIPROLIDINE HYDROCHLORIDEActive
Strength: 2.5 MG / TAB
Monograph: TRIPROLIDINE HYDROCHLORIDE

MedPath

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

© 2025 MedPath, Inc. All rights reserved.