MedPath

TRIPACEL HYBRID

TRIPACEL HYBRID

Discontinued
DIN Number

02224143

Drug Class

Human

Market Date

Jan 23, 1997

Company
HC

Sanofi Pasteur Limited

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 Number02224143
AIG Number0628682001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Schedule D
A
ATC Code
J07AJ52 PERTUSSIS, PURIFIED ANTIGEN, COMB. WITH TOXOIDS
Product Specifications
Dosage FormSuspension
Route of AdministrationIntramuscular
AHFS Classification80:08.00
Health Canada Classification

ACTIVE INGREDIENTS (6)

DIPHTHERIA TOXOIDActive
Strength: 15 LF / 0.5 ML
Monograph: DIPHTHERIA TOXOID
FILAMENTOUS HAEMAGGLUTININActive
Strength: 20 MCG / 0.5 ML
Monograph: FILAMENTOUS HAEMAGGLUTININ
FIMBRIAEActive
Strength: 5 MCG / 0.5 ML
Monograph: FIMBRIAE
PERTACTINActive
Strength: 3 MCG / 0.5 ML
Monograph: PERTACTIN
PERTUSSIS TOXOIDActive
Strength: 20 MCG / 0.5 ML
Monograph: PERTUSSIS TOXOID
TETANUS TOXOIDActive
Strength: 5 LF / 0.5 ML
Monograph: TETANUS TOXOID

MedPath

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

© 2025 MedPath, Inc. All rights reserved.