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:

2023-03-31

Original market date: See footnote 1

1993-12-31

Lot number: See footnote 2

LS6EH82

Expiry date: See footnote 2

2023-09-30

Product name:

NOVOLIN GE 40/60 PENFILL

Description:

3 ML 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:

02024314

Product Monograph/Veterinary Labelling:

Date: 2021-08-12 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):

Suspension

Route(s) of administration:

Subcutaneous

Number of active ingredient(s):

2

Schedule(s):

Schedule D

 

American Hospital Formulary Service (AHFS): See footnote 3

68:20.08 

Anatomical Therapeutic Chemical (ATC): See footnote 4

A10AD01 INSULIN (HUMAN)

Active ingredient group (AIG) number:See footnote5

0223312005

List of active ingredient(s)
Active ingredient(s) Strength
INSULIN INJECTION HUMAN BIOSYNTHETIC 40 UNIT / ML
INSULIN ISOPHANE HUMAN BIOSYNTHETIC 60 UNIT / ML
Version 4.0.2
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