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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:

2019-09-19

Original market date: See footnote 1

2019-09-19

Product name:

LEUCOVORIN CALCIUM INJECTION

Description:

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:

02480042

Product Monograph/Veterinary Labelling:

Date: 2020-03-06 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

GENERIC MEDICAL PARTNERS INC
1500 Don Mills Road, Suite 406
Toronto
Ontario
Canada  M3B 3K4

Class: 

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous,  Intramuscular

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

92:12.00   ANTIDOTES

Anatomical Therapeutic Chemical (ATC): See footnote 4

V03AF03  CALCIUM FOLINATE

Active ingredient group (AIG) number:See footnote 5

0108436002

List of active ingredient(s)
Active ingredient(s) Strength
LEUCOVORIN (LEUCOVORIN CALCIUM) 10 MG / ML

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