Current status:
Cancelled Post Market
Current status date:
2004-07-30
Product name:
ORUDIS E-50
DIN:
01926381
Electronic product monograph is not available
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
List of active ingredient(s)
Active ingredient(s) |
Strength |
KETOPROFEN
|
50 MG
|