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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:

2018-01-11

Original market date: See footnote 1

2010-09-23

Product name:

VANCOMYCIN HYDROCHLORIDE FOR INJECTION USP

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:

02342855

Product Monograph/Veterinary Labelling:

Date: 2018-11-05 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

STERIMAX INC
2770 Portland Drive
Oakville
Ontario
Canada  L6H 6R4

Class: 

Human

Dosage form(s):

Powder For Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

08:12.28.16   GLYCOPEPTIDES

Anatomical Therapeutic Chemical (ATC): See footnote 4

J01XA01  VANCOMYCIN

Active ingredient group (AIG) number:See footnote 5

0131315003

List of active ingredient(s)
Active ingredient(s) Strength
VANCOMYCIN (VANCOMYCIN HYDROCHLORIDE) 500 MG / VIAL

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