| Human medicinal products | | | SPC PL |  | Veterinary medicinal
products | | SPC PL | | | Herbal medicinal products | | | SPC PL | | Name of the medicinal
product |
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Package Leaflets (PL) for Human medicinal products
The package leaflet (PL) provides users with information about the medicinal product and its correct use. The package leaflets contain instructions in both Finnish and Swedish.
The package leaflets can be searched from alphabetical list, with the name, marketing authorisation number and the Anatomical Therapeutic Chemical, i.e. ATC Code of the Summary of Product Characteristics, SPC.
The package leaflets processed as part of the EU centralised marketing authorisation procedure are published by the European Medicines Agency, EMA.
Fimea's service contains links to the documents on medicinal products (EPAR PI) on the EMA website.
Drugs belonging to the centralised authorisation procedure can be searched in Fimea's service by using an alphabetical list or by entering the product name or ATC code.
The material being published is not necessarily complete or up-to-date due to the technical quality of files submitted to the Finnish Medicines Agency Fimea or earlier to the National Agency for Medicines and the delays in delivery. For this reason, Fimea cannot guarantee that the document on the Internet fully complies with the summary of product characteristics and package leaflet officially approved by a desicion for a marketing authorisation. Only the hard copies of the SPCs and the PLs, which are in accordance with the marketing authorisation, are conclusive.
| Product Information Leaflets 1 - 30 of 203 |
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supply | Name of the medicinal product |
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European Medicines Agency's website:
Iasibon - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Ibandronat Stada 150 mg tabletti, kalvopäällysteinen PL 2022-12-01
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SPC
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Resepti
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Ibandronate ratiopharm 150 mg tabletti, kalvopäällysteinen PL 2022-09-23
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SPC
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Resepti
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Ibandronate ratiopharm 50 mg tabletti, kalvopäällysteinen PL 2020-02-04
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European Medicines Agency's website:
Ibandronic acid Accord - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Ibandronic Acid Sandoz - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Ibandronic Acid Teva - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Ibrance - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Ibrance - EMA: EPAR PI
Finnish Swedish
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SPC
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Itsehoito
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Ibulinecaps 400mg kapseli, pehmeä pakkausseloste 2024-08-22.docx
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SPC
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Itsehoito
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Ibumax 200 mg, 400 mg tabletti, kalvopäällysteinen PL 2024-10-02 OTC
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SPC
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Resepti
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Ibumax 200 mg, 400 mg, 600 mg, 800 mg tabletti, kalvopäällysteinen PL 2024-10-02
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SPC
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Resepti
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Ibumax 200 mg, 400 mg, 600 mg, 800 mg tabletti, kalvopäällysteinen PL 2024-10-02
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SPC
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Resepti
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Ibumax Lysin 400 mg tabletti, kalvopäällysteinen PL 2024-10-03
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SPC
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Itsehoito
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Ibumax Lysin 400 mg tabletti, kalvopäällysteinen PL 2024-10-03 OTC
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SPC
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Itsehoito
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Ibumax-C 400 mg - 300 mg tabletti, kalvopäällysteinen PL 2024-10-03
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SPC
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Resepti
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Ibumetin 600 mg tabletti, kalvopäällysteinen PL 2024-05-10
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SPC
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Resepti
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Ibuprofen Accord 400 mg tabletti, kalvopäällysteinen PL 2024-03-13
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SPC
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Resepti
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Ibuprofen Accord 600 mg tabletti, kalvopäällysteinen PL 2024-03-13
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SPC
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Resepti
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Ibuprofen B. Braun 200 mg infuusioneste, liuos PL 2024-05-07
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SPC
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Resepti
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Ibuprofen B. Braun 400 mg infuusioneste, liuos PL 2024-01-19
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SPC
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Resepti
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Ibuprofen B. Braun 600 mg infuusioneste, liuos PL 2024-01-19
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SPC
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Itsehoito
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Ibuprofen Farmalider 20 mg - ml oraalisuspensio PL 2024-10-24 OTC
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SPC
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Resepti
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Ibuprofen Farmalider 40 mg - ml oraalisuspensio PL 2024-10-24
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European Medicines Agency's website:
Ibuprofen Gen.Orph - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Ibuprofen Strides 200 mg tabletti, kalvopäällysteinen PL 2024-08-09
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SPC
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Itsehoito
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Ibuprofen Strides 200 mg tabletti, kalvopäällysteinen PL OTC 2024-08-09
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SPC
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Resepti
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Ibuprofen Strides 400 mg tabletti, kalvopäällysteinen PL 2024-08-09
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SPC
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Itsehoito
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Ibuprofen Strides 400 mg tabletti, kalvopäällysteinen PL OTC 2024-08-09
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SPC
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Resepti
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Ibuprofen Strides 600 mg tabletti, kalvopäällysteinen PL 2024-08-09
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