Product information
From Health Canada
The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.
Current status:
Marketed
Current status date:
2017-07-14
Original market date: See footnote 1
1990-12-31
Product name:
SUPRAX
DIN:
00868965
Product Monograph/Veterinary Labelling:
Date:
2020-03-17
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
ODAN LABORATORIES LTD
325 Stillview Avenue
Pointe-Claire
Quebec
Canada
H9R 2Y6
Class:
Human
Dosage form(s):
Powder For Suspension
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
08:12.06.12
Anatomical Therapeutic Chemical (ATC): See footnote 4
J01DD08 CEFIXIME
Active ingredient group (AIG) number:See footnote5
0122105001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| CEFIXIME | 100 MG / 5 ML |