State Institute for Drug Control

Below are the lists of medicinal products whose marketing authorisations have ceased to be valid due to application of Section 34a of Act No. 378/2007 Coll., on Pharmaceuticals, as amended (the sunset clause). The person who held the marketing authorisation is obliged to withdraw these medicinal products from circulation without delay

• SC list of medicinal products whose marketing authorisation ceased to be valid 1.1.2024_1st version.xlsx, soubor typu xlsx, (16.45 kB) (update 25. 1. 2024)

• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2023.xlsx, soubor typu xlsx, (17.38 kB) (update 31. 1. 2023)

• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2022_2nd version.xlsx, soubor typu xlsx, (17.1 kB) (update 18. 5. 2022)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2022_1st version.xlsx, soubor typu xlsx, (17.13 kB) (update 31. 1. 2022)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2021 - 3rd version.xlsx, soubor typu xlsx, (21.45 kB) (update 23. 6. 2021)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2021 - 2nd version.xlsx, soubor typu xlsx, (21.33 kB) (update 15. 2. 2021)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2021 - 1st version.xlsx, soubor typu xlsx, (21.63 kB) (update 29. 1. 2021)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2020 - 4th version.xlsx, soubor typu xlsx, (18.92 kB) (update 21. 5. 2020)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2020 - 3rd version.xlsx, soubor typu xlsx, (18.78 kB) (update 5. 3. 2020)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2020 - 2nd version.xlsx, soubor typu xlsx, (18.88 kB) (update 6. 2. 2020)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2020 - 1st version.xlsx, soubor typu xlsx, (19.04 kB) (udate 31. 1. 2020)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2019 - 2nd version.xls, soubor typu xls, (56 kB) (update 7. 3. 2019)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2019 - 1st version..xls, soubor typu xls, (55.5 kB) (update 30. 1. 2019)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2018 - 5rd version.xls, soubor typu xls, (63 kB) (update 29. 11. 2018)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2018 - 4rd version.xls, soubor typu xls, (63.5 kB) (update 3. 10. 2018)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2018 - 3rd version.xls, soubor typu xls, (63 kB) (update 27. 4. 2018)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2018 - 2nd version.xls, soubor typu xls, (63.5 kB) (update 21. 2. 2018)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2018 - 1st version.xls, soubor typu xls, (62.5 kB) (update 31. 1. 2018)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2017 - 2nd version.xls, soubor typu xls, (60.5 kB) (update 15. 2. 2017)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2017 - 1st version.xls, soubor typu xls, (60.5 kB) (update 31. 1. 2017)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2016 - 4th version.xls, soubor typu xls, (63 kB) (update 7. 3. 2016)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2015 - 4rd version.xls, soubor typu xls, (69 kB) (update 27. 3. 2015)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1.1.2014 version 4.xls, soubor typu xls, (223.5 kB) (update 28.4.2014)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 4 2013 version 2.xls, soubor typu xls, (100 kB)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 3 2013 version 1.xls, soubor typu xls, (98.5 kB) (update 29.3.2013)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 2 2013 version 1.xls, soubor typu xls, (41.5 kB) (update 28.2.2013)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 1 2013 version 2.xls, soubor typu xls, (55.5 kB) (update 7.2.2013)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 12 2012 version 2.xls, soubor typu xls, (32 kB) (update 11.1.2013)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 11 2012 version 1.xls, soubor typu xls, (24.5 kB) (update 30.11.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 10 2012 version 2.xls, soubor typu xls, (66 kB) | (update 4.1.2013)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 9 2012 version 1.xls, soubor typu xls, (98.5 kB) (update 27.9.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 8 2012 version 2.xls, soubor typu xls, (113.5 kB) (update 12.9.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 7 2012 version 1.xls, soubor typu xls, (84.5 kB) (update 31.7.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 6 2012 version 1.xls, soubor typu xls, (36 kB) (update 29.6.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 5 2012 version 1.xls, soubor typu xls, (47 kB) (update 31.5.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 4 2012 version 2.xls, soubor typu xls, (69.5 kB) (update 14.5.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 3 2012 version 2.xls, soubor typu xls, (84 kB) (update 20.4.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 2 2012 version 1.xls, soubor typu xls, (88.5 kB) (update 29.2.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 1 2012 version 2.xls, soubor typu xls, (68 kB) (update 17.7.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 12 2011 version 1.xls, soubor typu xls, (70.5 kB) (update 29.12.2011)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 11 2011 version 2.xls, soubor typu xls, (108 kB)
  (update 30. 11. 2011)
• SC_list of medicinal products whose marketing authorisation has ceased to be valid 1.10.2011_version 2, soubor typu xls, (56.5 kB)
  (update 25.1.2012)
• SC list of medicinal products whose marketing authorisation has ceased to be valid 1. 9. 2011 version 1, soubor typu xls, (38 kB) (update 4. 10. 2011)
• SC_list of medicinal products whose marketing authorisation has ceased to be valid 1.8.2011_version3.xls, file type xls, (95.5 kB)
  (update 10. 1. 2012) 
• SC_list of medicinal products whose marketing authorisation has ceased_to be valid 1_7_2011_version 5.xls, file type xls, (133.5 kB)(update 10. 1. 2012) 
• SC_list of medicinal products whose marketing authorisation has ceased to be valid 1_6_2011_version 1, soubor typu xls, (85,5 kB) (update 22. 6. 2011)

• SC list of medicinals products whose marketing authorisation has caesed to be valid 1 5 2011 version 5.xls, soubor typu xls, (113.5 kB) (update 29.2.2012)

• SC list of medicinal products whose marketing authorisation has ceased to be valid 1 4 2011 version 7, soubor typu xls, (110 kB) (update 3. 1. 2012)

• SC list of medicinals products whose marketing authorisation has caesed to be valid 1 1 2011 version 12.xls, soubor typu xls, (509.5 kB) (update 29.2.2012)

• SC_list of medicinal products whose marketing authorisation has ceased to be valid 1.10.2011_version1, soubor typu xls, (57.5 kB) (update 31.10.2011)

Marketing Authorisation Branch
17. 2. 2011