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

Current status date:

2011-01-08

Original market date: See footnote 1

1993-12-31

Product name:

NOVOLIN GE 30/70

Description:

10 ML VIAL

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DIN:

02024217

Product Monograph/Veterinary Labelling:

Date: 2019-07-26 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

0223312003

List of active ingredient(s)
Active ingredient(s) Strength
INSULIN INJECTION HUMAN BIOSYNTHETIC 30 UNIT / ML
INSULIN ISOPHANE HUMAN BIOSYNTHETIC 70 UNIT / ML
Version 4.0.2
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