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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:

2020-02-12

Original market date: See footnote 1

2020-02-12

Product name:

IVOZFO

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:

02488086

Product Monograph/Veterinary Labelling:

Date: 2019-05-01 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

VERITY PHARMACEUTICALS INC.
2560 Matheson Blvd. E., Suite 220
Mississauga
Ontario
Canada  L4W 4Y9

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

08:36.00   URINARY ANTI-INFECTIVES

Anatomical Therapeutic Chemical (ATC): See footnote 4

J01XX01  FOSFOMYCIN

Active ingredient group (AIG) number:See footnote 5

0137036004

List of active ingredient(s)
Active ingredient(s) Strength
FOSFOMYCIN (FOSFOMYCIN SODIUM) 4 G / VIAL

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