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:
TECHNELITE
Description:
18.5 TO 740 GBQ
DIN:
02328550
Product Monograph/Veterinary Labelling:
Date:
2009-06-02
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
LANTHEUS MI CANADA INC
1111 Dr. Frederik-Philips Blvd., Suite 600
Montreal
Quebec
Canada
H4M 2X6
Class:
Radiopharmaceutical
Dosage form(s):
Solution
Route(s) of administration:
Oral , Instillation , Intravenous
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
V09 DIAGNOSTIC RADIOPHARMACEUTICALS
Active ingredient group (AIG) number:See footnote5
0152593006
| Active ingredient(s) | Strength |
|---|---|
| TECHNETIUM TC 99M | 740 GBQ / GEN |