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Intended for UK patients and members of the public

Prednisolone 25mg Tablets

Prednisolone 25mg Tablets

PL Number:
0142/0845
MA Holder:
Accord-UK Ltd
Product Classification:
POM
Product Status:
Active

Product Documentation

  • Description of update: To update sections 4.3, 4.4, 4.5, and 4.8 of the SmPC in line with the reference products Prednisolone Pfizer 2.5 mg, 5 mg, and 10 mg tablets (MAH: Pfizer AB, MA Number: 10059, 8822, 10060). The PIL has also been updated accordingly. In addition, the following updates have been included: Editorial and formatting updates to the PIL; Update to lactose excipient information in the PIL to align with EC Excipient Guidelines; QRD update to SmPC section 4.4 and the PIL.

    Date of approval: 11/08/2026

    PIL sections updated: Headline, 2, 3, 4, 5 and 6

  • Description of update: To update sections 4.3, 4.4, 4.5, and 4.8 of the SmPC in line with the reference products Prednisolone Pfizer 2.5 mg, 5 mg, and 10 mg tablets (MAH: Pfizer AB, MA Number: 10059, 8822, 10060). The PIL has also been updated accordingly. In addition, the following updates have been included: Editorial and formatting updates to the PIL; Update to lactose excipient information in the PIL to align with EC Excipient Guidelines; QRD update to SmPC section 4.4 and the PIL.

    Date of approval: 11/08/2026

    SmPC sections updated: 4.3, 4.4, 4.5, 4.8 and 10

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at yellowcard.mhra.gov.uk. By reporting side effects, you can help provide more information on the safety of this medicine.

Report a side effect or a product complaint

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