MedPath

LOMOTIL

LOMOTIL

Approved
DIN Number

00036323

Drug Class

Human

Market Date

Dec 31, 1960

Company
HC

Pfizer Canada Ulc

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 Number00036323
AIG Number0203532001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Narcotic (CDSA I)
A
ATC Code
A07DA01 DIPHENOXYLATE
Product Specifications
Dosage FormTablet
Route of AdministrationOral
AHFS Classification56:08.00
Health Canada Classification

ACTIVE INGREDIENTS (2)

ATROPINE SULFATEActive
Strength: .025 MG
Monograph: ATROPINE SULFATE
DIPHENOXYLATE HYDROCHLORIDEActive
Strength: 2.5 MG
Monograph: DIPHENOXYLATE HYDROCHLORIDE

MedPath

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

© 2025 MedPath, Inc. All rights reserved.