PHARMITUSSIN DM
PHARMITUSSIN DM
Discontinued
DIN Number
00632031
Drug Class
Human
Market Date
Dec 31, 1985
Company
HC
therapex division de e-z-em canada 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 Number00632031
AIG Number0200826001
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
R05FA02 OPIUM DERIVATIVES AND EXPECTORANTS
Product Specifications
Dosage FormSyrup
Route of AdministrationOral
AHFS Classification48:16.00
Health Canada Classification
ACTIVE INGREDIENTS (2)
DEXTROMETHORPHAN HYDROBROMIDEActive
Strength: 15 MG / 5 ML
Monograph: DEXTROMETHORPHAN HYDROBROMIDE
GUAIFENESINActive
Strength: 100 MG / 5 ML
Monograph: GUAIFENESIN