Product information

From Health Canada

New search

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:

2018-10-04

Original market date: See footnote 1

2015-08-10

Product name:

ENALAPRIL

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:

02442973

Product Monograph/Veterinary Labelling:

Date: 2019-01-25 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

SIVEM PHARMACEUTICALS ULC
4705 Dobrin Street
Saint-Laurent
Quebec
Canada  H4R 2P7

Class: 

Human

Dosage form(s):

Tablet

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Prescription  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

24:32.04   ANGIOTENSIN-CONVERTING ENZYME INHIBITORS

Anatomical Therapeutic Chemical (ATC): See footnote 4

C09AA02  ENALAPRIL

Active ingredient group (AIG) number:See footnote 5

0152325002

List of active ingredient(s)
Active ingredient(s) Strength
ENALAPRIL SODIUM (ENALAPRIL MALEATE) 8 MG

Application information

Related information

Contact us

Version 3.8.0
Date modified: