OMNI-TUSS SUS
OMNI-TUSS SUS
Discontinued
DIN Number
00815136
Drug Class
Human
Market Date
Dec 31, 1966
Company
HC
aventis 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 Number00815136
AIG Number0521133001
Classification & Schedule
C
Drug Class
Human
S
Schedule
Narcotic (CDSA I)
A
ATC Code
R05FA02 OPIUM DERIVATIVES AND EXPECTORANTS
Product Specifications
Dosage FormSuspension
Route of AdministrationOral
AHFS Classification48:08.00
Health Canada Classification
ACTIVE INGREDIENTS (5)
CHLORPHENIRAMINEActive
Strength: 3 MG / 5 ML
Monograph: CHLORPHENIRAMINE
CODEINEActive
Strength: 10 MG / 5 ML
Monograph: CODEINE
EPHEDRINE AS RESIN COMPLEXActive
Strength: 25 MG / 5 ML
Monograph: EPHEDRINE AS RESIN COMPLEX
GUAIACOL CARBONATEActive
Strength: 20 MG / 5 ML
Monograph: GUAIACOL CARBONATE
PHENYLTOLOXAMINEActive
Strength: 5 MG / 5 ML
Monograph: PHENYLTOLOXAMINE