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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:

1998-06-17

Original market date: See footnote 1

1996-09-10

Product name:

HEPARIN SODIUM 25000UNITS IN 5% DEXTROSE INJ

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:

02209721

Product Monograph/Veterinary Labelling:

Date: 2012-07-17 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

B. BRAUN MEDICAL INC
824 Twelfth Avenue
Bethlehem
Pennsylvania
United States  18018

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

2

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

B01AB51  HEPARIN, COMBINATIONS

Active ingredient group (AIG) number:See footnote 5

0220064003

List of active ingredient(s)
Active ingredient(s) Strength
DEXTROSE 5 G / 100 ML
HEPARIN SODIUM 10000 UNIT / 100 ML

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