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

Class not statedclass recorded on the notice
2025-07-07last updated
Drugscategory
Nomarked archived

What the notice records

Every field on this notice, as published
ProductNRA-Amlodipine 5 mg, DIN 02476460
IssueProduct safety
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 [email protected] 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.
CategoryDrugs
Publishing bodyCommunications and Public Affairs Branch
ClassClass not stated
Last updated2025-07-07

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