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:
1998-06-17
Original market date: See footnote 1
1996-09-10
Product name:
HEPARIN SODIUM 25000UNITS IN 5% DEXTROSE INJ
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
American Hospital Formulary Service (AHFS): See footnote 3
20:12.04.16
Anatomical Therapeutic Chemical (ATC): See footnote 4
B01AB51 HEPARIN, COMBINATIONS
Active ingredient group (AIG) number:See footnote5
0220064003
| Active ingredient(s) | Strength |
|---|---|
| DEXTROSE | 5 G / 100 ML |
| HEPARIN SODIUM | 10000 UNIT / 100 ML |