Sandoz Pty Ltd — Amlodipine Sandoz 5mg tablets

What are the defects?

This medicine may have been dispensed with missing blister sheets.

What are the hazards?

Affected packs may not contain the correct number of tablets.

What should consumers do?

If you or someone you provide care for takes Amlodipine Sandoz tablets, please check the batch number (displayed on the packs and blister sheets) to see if it is affected by this recall.

If you have a pack that has been affected by this issue, return any unused medicine to your pharmacy for a refund. If there are no anomalies with your product, you can choose to continue using it as normal.

If you have any other questions or concerns about this issue, talk to your health professional or contact Sandoz Pty Ltd on 1800 726 369.

Supplier
Sandoz
Where the product was sold
Nationally

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category