Caltrate 500 mg / 1000 IU, chewable tablets
- Name:
Caltrate 500 mg / 1000 IU, chewable tablets
- Company:
GlaxoSmithKline Consumer Healthcare (Ireland) Ltd
- Active Ingredients:
- Legal Category:
Supply through pharmacy only
Patient Information Leaflet Patient Information Leaflet last updated on medicines.ie: 03/03/21

Summary of Product Characteristics last updated on medicines.ie: 3/3/2021
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GlaxoSmithKline Consumer Healthcare (Ireland) Ltd
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When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.
Updated on 3 March 2021 SPC
Reasons for updating
- Change to section 2 - Qualitative and quantitative composition
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Updated on 3 March 2021 PIL
Reasons for updating
- Change to section 2 - excipient warnings
- Change to section 6 - date of revision
Updated on 30 November 2020 SPC
Reasons for updating
- Change to section 7 - Marketing authorisation holder
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Updated on 30 November 2020 PIL
Reasons for updating
- Change to section 6 - marketing authorisation holder
- Change to section 6 - date of revision
Updated on 11 March 2019 PIL
Reasons for updating
- New PIL for new product
Updated on 11 March 2019 SPC
Reasons for updating
- New SPC for new product
Legal category: Supply through pharmacy only