Product information
From Health Canada
Current status:
Cancelled Post Market
Current status date:
2005-07-19
Original market date: See footnote 1
2000-10-11
Product name:
IBUPROFEN
DIN:
02242408 Electronic product monograph is not available
Company:
D.C. LABS LIMITED
191 Mcnabb Street
Markham
Ontario
Canada
L3R 5V7
Class:
Human
Dosage form(s):
Tablet
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
OTC
American Hospital Formulary Service (AHFS): See footnote 3
28:08.04.92
Anatomical Therapeutic Chemical (ATC): See footnote 4
M01AE01 IBUPROFEN
Active ingredient group (AIG) number:See footnote5
0108883004
Active ingredient(s) | Strength |
---|---|
IBUPROFEN | 200 MG / TAB |