Home/Recalls/CANADA-77675
Health CanadaGeneral Alert

NRA-Amlodipine 5 mg tablets: One lot recalled as some bottles may contain the wr...

Published: July 7, 2025Recall ID: 77675Category: generalCountry: Canada

Reason for Recall / Hazard

Product safety

Product Description & Identification

Check your medication bottle to ensure it only contains NRA-AMLODIPINE 5 mg tablets.If your bottle contains any round tablets, which are not the correct shape, or if you're unsure, return the bottle to your pharmacy for a replacement.If you are unable to get a replacement immediately, continue to take your medication as directed, but do not take the round tablets as these are the wrong medication.Contact your health care professional if you are dizzy, have unusually low blood pressure or slow heartbeats. If you are unable to access a health care professional and you are experiencing these symptoms, call 911.If you have questions about this recall, contact Nora Pharma Inc. by calling their Quality Assurance Department at 450-904-2355 or by emailing info@norapharma.ca.Report any health product-related side effects or complaints to Health Canada.Additional information for health professionals:Health care professionals, such as pharmacists, should check packages and bottles labelled NRA-AMLODIPINE 5 mg (amlodipine besylate) before dispensing to make sure they do not contain Metoprolol Succinate prolonged-release 12.5 mg tablets. Report any unusual bottles or other issues to the company and Health Canada.

Affected Products

NRA-Amlodipine 5 mg, DIN 02476460

Additional Source Details

FieldValue
N I D77675
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/nra-amlodipine-5-mg-tablets-one-lot-recalled-some-bottles-may-contain-wrong-drug
IssueProduct safety
TitleNRA-Amlodipine 5 mg tablets: One lot recalled as some bottles may contain the wrong drug
ProductNRA-Amlodipine 5 mg, DIN 02476460
Archived0
CategoryDrugs
Last updated2025-07-07
OrganizationCommunications and Public Affairs Branch
What you should doCheck your medication bottle to ensure it only contains NRA-AMLODIPINE 5 mg tablets.If your bottle contains any round tablets, which are not the correct shape, or if you're unsure, return the bottle to your pharmacy for a replacement.If you are unable to get a replacement immediately, continue to take your medication as directed, but do not take the round tablets as these are the wrong medication.Contact your health care professional if you are dizzy, have unusually low blood pressure or slow heartbeats. If you are unable to access a health care professional and you are experiencing these symptoms, call 911.If you have questions about this recall, contact Nora Pharma Inc. by calling their Quality Assurance Department at 450-904-2355 or by emailing info@norapharma.ca.Report any health product-related side effects or complaints to Health Canada.Additional information for health professionals:Health care professionals, such as pharmacists, should check packages and bottles labelled NRA-AMLODIPINE 5 mg (amlodipine besylate) before dispensing to make sure they do not contain Metoprolol Succinate prolonged-release 12.5 mg tablets. Report any unusual bottles or other issues to the company and Health Canada.

Overview

  • Recalling FirmCommunications and Public Affairs Branch
Official Agency Alert