FOI release
Requesting information regarding the licensing of Ditropan Tablets in the UK/EU
Case reference FOI2025/00387
Received 22 April 2025
Published 23 July 2025
Request
Requesting information regarding Ditropan 2.5 mg and 5 mg tablets. Were these approved Europe wide and via a centralized or a MRP and is or was Northern Ireland listed as an concerned member state.
Response
see attached
Documents
This is Medicines and Healthcare products Regulatory Agency's response to a freedom of information (FOI) or environmental information regulations (EIR) request.
You can browse our other responses or make a new FOI request.