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:
2017-07-13
Original market date: See footnote 1
1977-12-31
Product name:
LIPIODOL ULTRA FLUID
Description:
38%
DIN:
00386685
Product Monograph/Veterinary Labelling:
Date:
2017-07-12
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
GUERBET
Bp 57400
Roissy Cdg Cedex
Val-D'Oise
France
95943
Class:
Human
Dosage form(s):
Liquid
Route(s) of administration:
Parenteral (Unspecified) , Intracavitary
Number of active ingredient(s):
1
Schedule(s):
Ethical
American Hospital Formulary Service (AHFS): See footnote 3
36:68.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
V08AD01 ETHYL ESTERS OF IODISED FATTY ACIDS
Active ingredient group (AIG) number:See footnote5
0103970041
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| IODINE (ETHIODIZED OIL) | 380 MG / G |