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:

Cancelled Post Market

Current status date:

2023-02-21

Original market date: See footnote 1

1998-03-08

Lot number: See footnote 2

16144629

Expiry date: See footnote 2

2025-08-31

Product name:

OMNIPAQUE 180

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section.

DIN:

02172720

Product Monograph/Veterinary Labelling:

Date: 2021-01-12 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

GE HEALTHCARE CANADA INC
1919 Minnesota Court
Mississauga
Ontario
Canada L5N 0C9

Class:

Human

Dosage form(s):

Solution

Route(s) of administration:

Subarachnoidal

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

V08AB02 IOHEXOL

Active ingredient group (AIG) number:See footnote5

0116846002

List of active ingredient(s)
Active ingredient(s) Strength
IOHEXOL 388 MG / ML
Version 4.0.2
Date modified: