Product information
From Health Canada
Current status:
Cancelled Post Market
Current status date:
2003-07-22
Original market date: See footnote 1
1987-12-31
Product name:
ORUDIS E-100
DIN:
01926365 Electronic product monograph is not available
Company:
AVENTIS PHARMA INC
2905 Place Louis-R. Renaud
Laval
Quebec
Canada
H7V 0A3
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) | Strength |
---|---|
KETOPROFEN | 100 MG |