Medicinal Products

Pemetreksed PharmaS 500 mg prašak za koncentrat za otopinu za infuziju

Name Pemetreksed PharmaS 500 mg prašak za koncentrat za otopinu za infuziju
Marketing Authorisation Number HR-H-101756271
Active Substance pemetrekseddinatrij hemipentahidrat
Composition jedna bočica sadrži 500 mg pemetrekseda (u obliku pemetrekseddinatrij hemipentahidrata)
Pharmaceutical Form prašak za koncentrat za otopinu za infuziju
Packaging [MA Number for Packaging] 1 bočica s praškom, u kutiji  [HR-H-101756271-01]
Manufacturer Synthon Hispania S.L., Barcelona, Španjolska
Synthon s.r.o., Blansko, Češka
Adamed Pharma S.A., Pabianice, Poljska
Marketing Authorisation Holder PharmaS d.o.o., Radnička cesta 47, Zagreb, Hrvatska
Marketing Authorisation Date 15.10.2020
MA Period of Validity unlimited
MA Revocation Date 04.09.2023*
Classification Number UP/I-530-09/20-02/15
Registration Number 381-12-01/30-20-05
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code L01BA04
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Marketing authorisation has been revoked by request of the marketing authorisation holder.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.

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