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KETOPROFEN-E ECT 100MG

KETOPROFEN-E ECT 100MG

Discontinued
DIN Number

02084198

Drug Class

Human

Market Date

Dec 31, 1996

Company
HC

PRO DOC LIMITEE

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 Number02084198
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 / ECT
Monograph: KETOPROFEN

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