ePrivacy and GPDR Cookie Consent by TermsFeed Generator

TEZEFORT

40MG/10MG TBL NOB 28

SPC - Summary of product characteristics tezefort-spc.pdf
NR - Registration decision NR5560614.pdf
PIL - Package leaflet tezefort-pil.pdf
PAR - Public assessment report tezefort-par.doc
Text on the wrap tezefort-obal.pdf
Braills Approved – name of the medicinal product in Braille on the packaging was confirmed.
SPCs and PILs of centralised medicinal products (registration number beginning EU) are included as a link to website of the European Medicines Agency (EMEA) Information is available on this website in section Product Information. Please note that the texts refer to all strenghts and pharmaceutical forms of the given medicinal product. SUKL is not responsible for update SPCs and PILs on EMEA web site.

EAN – more specific information about EAN code is available in the Overview

I - neregistrovaný léčivý přípravek jehož distribuce, výdej a použití je umožněno na základě opatření Ministerstva zdravotnictví ČR podle § 8 odst. 6 zákona o léčivech.

Back to list