Dona 1500 mg Powder for oral solution
- Licence status
- Withdrawn: 19/12/2025
- Active substances
- Glucosamine sulfate, Sodium chloride
- Dosage Form
- Powder for oral solution
- Licence number
- PPA23176/035/001
- Licence holder
- Lexon Pharmaceuticals (Ireland) Limited
Product documents
- Package Leaflet
- Summary of Product Characteristics
- Public Assessment Report
Licence information
- ATC code
- M01AX Other antiinflammatory and antirheumatic agents, non-steroids, M01AX05 glucosamine
- Legal supply status
- Product not subject to medical prescription
- Place of sale
- Supply through pharmacies only
- Marketing availability
- Unknown
- Advertising conditions
- Advertising to the general public
- Licence issued
- 18/09/2020