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Intended for UK patients and members of the public

Trimethoprim Tablets

Active Ingredients

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

Trimethoprim Tablets BP 200mg

PL Number:
0142/0225
MA Holder:
Accord-UK Ltd
Product Classification:
POM
Product Status:
Active

Product Documentation

  • Description of update: 1) To register section 3.2.P.7 of the dossier to reflect details of the blister packaging material. 2) To remove reference to the heat seal lacquer from section 6.5 of the SmPC.

    There have been no changes to the blister packaging material itself, only an update in the supporting dossier details. There are no changes to the leaflet and labelling text.

    SmPC section(s) updated– 6.5, 10

    No changes to artwork

  • Variation Description: To update sections 4.4, 4.5, 4.6, 4.8 and 5.2 of the SmPC in line with the reference product, Trimethoprim 100mg Tablets (PL 06453/0043, MAH: Athlone Laboratories Limited) dated 16th June 2022. Consequently, the PIL has been updated. In addition, section 2 of the SmPC has been updated to follow the standard QRD wording at the request of the MHRA.

    PIL sections updated – 2, 4, 5 and 6.

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

General FAQs

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