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ALTI-MEXILETINE

ALTI-MEXILETINE

Discontinued
DIN Number

02231690

Drug Class

Human

Market Date

Nov 7, 1997

Company
HC

altimed pharma 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 Number02231690
AIG Number0116151001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
C01BB02 MEXILETINE
Product Specifications
Dosage FormCapsule
Route of AdministrationOral
AHFS Classification24:04.04.08
Health Canada Classification

ACTIVE INGREDIENTS (1)

MEXILETINE HYDROCHLORIDEActive
Strength: 100 MG
Monograph: MEXILETINE HYDROCHLORIDE

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