MedPath

SUBOXONE

SUBOXONE

Approved
DIN Number

02295695

Drug Class

Human

Market Date

Nov 26, 2007

Company
HC

INDIVIOR UK 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 Number02295695
AIG Number0252216001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Narcotic (CDSA I)
A
ATC Code
N07BC51 BUPRENORPHINE, COMBINATIONS
Product Specifications
Dosage FormTablet
Route of AdministrationSublingual
AHFS Classification28:10.00
Health Canada Classification

ACTIVE INGREDIENTS (2)

BUPRENORPHINE (BUPRENORPHINE HYDROCHLORIDE)Active
Strength: 2 MG
Monograph: BUPRENORPHINE (BUPRENORPHINE HYDROCHLORIDE)
NALOXONE (NALOXONE HYDROCHLORIDE DIHYDRATE)Active
Strength: 0.5 MG
Monograph: NALOXONE (NALOXONE HYDROCHLORIDE DIHYDRATE)

MedPath

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

© 2025 MedPath, Inc. All rights reserved.