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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:

2011-01-08

Original market date: See footnote 1

1993-12-31

Product name:

NOVOLIN GE TORONTO PENFILL

Description:

3ML PENFILL CARTRIDGE

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:

02024284

Product Monograph/Veterinary Labelling:

Date: 2016-03-11 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

NOVO NORDISK CANADA INC
101-2476 Argentia Road
Mississauga
Ontario
Canada  L5N 6M1

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous,  Subcutaneous,  Intramuscular

Number of active ingredient(s):

1

Schedule(s):

Schedule D  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

68:20.08   INSULINS

Anatomical Therapeutic Chemical (ATC): See footnote 4

A10AB01  INSULIN (HUMAN)

Active ingredient group (AIG) number:See footnote 5

0123340001

List of active ingredient(s)
Active ingredient(s) Strength
INSULIN INJECTION HUMAN BIOSYNTHETIC 100 UNIT / ML

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