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:

INDIUM DTPA IN 111

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:

02329093

Product Monograph/Veterinary Labelling:

Date: 2018-06-07 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

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

Class:

Radiopharmaceutical

Dosage form(s):

Solution

Route(s) of administration:

Intrathecal

Number of active ingredient(s):

1

Schedule(s):

Schedule C

 

American Hospital Formulary Service (AHFS): See footnote 3

36:68.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

V09AX01 INDIUM 111 IN PENTETIC ACID

Active ingredient group (AIG) number:See footnote5

0152616001

List of active ingredient(s)
Active ingredient(s) Strength
PENTETATE INDIUM DISODIUM IN 111 37 MBq / ML
Version 4.0.2
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