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:
2023-04-14
Original market date: See footnote 1
1993-12-31
Product name:
BURINEX
DIN:
00728276
Product Monograph/Veterinary Labelling:
Date:
2022-07-19
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
KARO PHARMA AB
Klara Norra Kyrkogata 33
Stockholm
--
Sweden
11122
Class:
Human
Dosage form(s):
Tablet
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
40:28.08
Anatomical Therapeutic Chemical (ATC): See footnote 4
C03CA02 BUMETANIDE
Active ingredient group (AIG) number:See footnote5
0119025001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| BUMETANIDE | 5 MG |