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:
2001-09-20
Original market date: See footnote 1
1994-12-31
Product name:
ULTRACAINE D-S INJECTION
DIN:
01988530
Product Monograph/Veterinary Labelling:
Date:
2014-01-27
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
HANSAMED LIMITED
2830 Argentia Rd., Units 7-9
Mississauga
Ontario
Canada
L5N 8G4
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Block/Infiltration
Number of active ingredient(s):
2
Schedule(s):
Ethical
American Hospital Formulary Service (AHFS): See footnote 3
72:00.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
N01BB58 ARTICAINE, COMBINATIONS
Active ingredient group (AIG) number:See footnote5
0226661002
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| ARTICAINE HYDROCHLORIDE | 40 MG / ML |
| EPINEPHRINE | 5 MCG / ML |