ORUDIS E-100
ORUDIS E-100
Discontinued
DIN Number
01926365
Drug Class
Human
Market Date
Dec 31, 1987
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 Number01926365
AIG Number0110497002
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
M01AE03 KETOPROFEN
Product Specifications
Dosage FormTablet (Enteric-Coated)
Route of AdministrationOral
AHFS Classification28:08.04.92
Health Canada Classification
ACTIVE INGREDIENTS (1)
KETOPROFENActive
Strength: 100 MG
Monograph: KETOPROFEN