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

Product name:

DRAX EXAMETAZIME

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:

02495848

Product Monograph/Veterinary Labelling:

Date: 2020-01-23 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

JUBILANT DRAXIMAGE INC. DBA JUBILANT RADIOPHARMA
16751 Trans Canada Hwy
Kirkland
Quebec
Canada H9H 4J4

Class:

Radiopharmaceutical

Dosage form(s):

Powder For Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

1

Schedule(s):

Schedule C

 

American Hospital Formulary Service (AHFS): See footnote 3

Anatomical Therapeutic Chemical (ATC): See footnote 4

 

Active ingredient group (AIG) number:See footnote5

0152612001

List of active ingredient(s)
Active ingredient(s) Strength
EXAMETAZIME 0.5 MG / VIAL
Version 4.0.2
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