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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:

2016-11-17

Original market date: See footnote 1

2016-11-17

Product name:

HEPARIN SODIUM INJECTION USP

Description:

SINGLE DOSE PREFILLED SYRINGE

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:

02456958

Product Monograph/Veterinary Labelling:

Date: 2021-01-11 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

STERINOVA INC.
3005 Avenue Jose-Maria Rosell
Saint-Hyacinthe
Quebec
Canada  J2S 0J9

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Subcutaneous

Number of active ingredient(s):

1

Schedule(s):

Ethical  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

20:12.04.16   HEPARINS

Anatomical Therapeutic Chemical (ATC): See footnote 4

B01AB01  HEPARIN

Active ingredient group (AIG) number:See footnote 5

0104596002

List of active ingredient(s)
Active ingredient(s) Strength
HEPARIN SODIUM 5000 UNIT / 0.5 ML

Application information

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