Medicinal Products

Dotagraf LV 0,5 mmol/ml otopina za injekciju

Name Dotagraf LV 0,5 mmol/ml otopina za injekciju
Marketing Authorisation Number HR-H-254395217
Active Substance meglumingadoterat
Composition 1 ml otopine za injekciju sadrži 279,32 mg gadoteratne kiseline (u obliku megluminske soli), što odgovara 0,5 mmol
Pharmaceutical Form otopina za injekciju
Manufacturer Sanochemia Pharmazeutika GmbH, Neufeld An Der Leitha, Austrija
Marketing Authorisation Holder Bayer d.o.o., Radnička cesta 80, Zagreb, Hrvatska
Marketing Authorisation Date 27.11.2019
MA Period of Validity unlimited
MA Revocation Date 08.08.2023*
Classification Number UP/I-530-09/19-02/184
Registration Number 381-12-01/30-19-03
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code V08CA02
Medicinal product marketed in the Croatia Trajni prekid opskrbe
SmPC download
PL download
Public Assessment Report download

*Note

Marketing authorisation has been revoked by request of the marketing authorisation holder. In accordance with Article 113 of Medicinal Products Act (Official Gazette No. 76/13), only a medicinal product in respect of which a marketing authorisation has been granted by the Agency for Medicinal Products and Medical Devices or the European Commision, and a medicinal product in respect of which an authorisation for parallel import or parallel distribution has been granted may be placed on the market of the Republic of Croatia. By way of derogation from this provision, a batch of medicinal product may be on the market for no longer than 18 months following the expiry of revocation of the marketing authorisation, unless its shelf life expires first.

Packaging

Direct Healthcare Professional Communication

Name Date Download
Pismo zdravstvenim radnicima o najnovijim preporukama za gadolinijska kontrastna sredstva 04.12.2017 Bayer d.o.o., Bracco Imaging S.p.A., GE Healthcare d.o.o. i Pharmacol d.o.o.
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