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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:

2012-03-19

Original market date: See footnote 1

2012-03-19

Product name:

HALAVEN

Description:

2ML SINGLE USE VIAL

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:

02377438

Product Monograph/Veterinary Labelling:

Date: 2017-08-04 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

EISAI LIMITED
6925 Century Ave, Suite 701
Mississauga
Ontario
Canada  L5N 7K2

Class: 

Human

Dosage form(s):

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

10:00.00   ANTINEOPLASTIC AGENTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

L01XX41  ERIBULIN

Active ingredient group (AIG) number:See footnote 5

0153064001

List of active ingredient(s)
Active ingredient(s) Strength
ERIBULIN MESYLATE 0.5 MG / ML

Risk Management Plans See footnote 7

A Risk Management Plan (RMP) for this product was submitted.

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