Product information
From Health Canada
Current status:
Cancelled Post Market
Current status date:
2009-07-23
Original market date: See footnote 1
1996-12-31
Product name:
KETOPROFEN-E ECT 100MG
DIN:
02084198 Electronic product monograph is not available
Company:
PRO DOC LIMITEE
2925 Boulevard Industriel
Laval
Quebec
Canada
H7L 3W9
Class:
Human
Dosage form(s):
Tablet (Enteric-Coated)
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
28:08.04.92
Anatomical Therapeutic Chemical (ATC): See footnote 4
M01AE03 KETOPROFEN
Active ingredient group (AIG) number:See footnote5
0110497002
Active ingredient(s) See footnote8 | Strength |
---|---|
KETOPROFEN | 100 MG / ECT |