FOI release

UK market Authorization information

Some or all of the information requested was not provided because we determined that the cost to do so would exceed the appropriate limit.

Case reference FOI2025/01211

Received 17 November 2025

Published 31 December 2025

Request

I am requesting a complete, machine-readable dataset of all UK marketing authorisations (MAs) for human medicines held by the MHRA. Specifically, I would like the following information for every product licence (PL / PLGB / PLNI) from the earliest date available up to the present: • Product Licence Number (PL, PLGB, or PLNI) • Product name • Active substance(s) • Marketing Authorisation Holder (MAH) • Date of first authorisation in the UK • Dates of subsequent variations, renewals, suspensions, revocations, or withdrawals (if available) • Current status of each licence (e.g. active, suspended, withdrawn) • Pharmaceutical form and strength (if available) I would like this information in a machine-readable format such as CSV or Excel. If different datasets exist for historical and current licences, please include both or as much as is reasonably available. This request covers human medicines only (not veterinary).

Response

See attached

Documents

• FOI2025_00058 All MAs.pdf (4.9 MB)
• FOI2025_01211 (redacted).pdf (854.5 KB)

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.