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