MedPath

TUSSIONEX

TUSSIONEX

Discontinued
DIN Number

01916963

Drug Class

Human

Market Date

Dec 31, 1957

Company
HC

sanofi-aventis 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 Number01916963
AIG Number0252486001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Narcotic (CDSA I)
A
ATC Code
R05DA20 COMBINATIONS
Product Specifications
Dosage FormTablet (Extended-Release)
Route of AdministrationOral
AHFS Classification04:04.04
Health Canada Classification

ACTIVE INGREDIENTS (2)

HYDROCODONEActive
Strength: 5 MG
Monograph: HYDROCODONE
PHENYLTOLOXAMINEActive
Strength: 10 MG
Monograph: PHENYLTOLOXAMINE

MedPath

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

© 2025 MedPath, Inc. All rights reserved.