NEBIVOLOLO RATIOPHARM

Valsts: Itālija

Valoda: itāļu

Klimata pārmaiņas: AIFA (Agenzia Italiana del Farmaco)

Aktīvā sastāvdaļa:

Nebivololo

Pieejams no:

RATIOPHARM GMBH

ATĶ kods:

C07AB12

SNN (starptautisko nepatentēto nosaukumu):

Nebivolol

Vienības iepakojumā:

" 5 MG COMPRESSE " 10 COMPRESSE IN BLISTER PVC/AL; " 5 MG COMPRESSE " 100 COMPRESSE IN BLISTER PVC/AL; " 5 MG COMPRESSE " 14 COM

Klase:

M

Ārstniecības joma:

Nebivololo

Produktu pārskats:

039429143 - 5 MG COMPRESSE 500 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429055 - 5 MG COMPRESSE 28 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429129 - 5 MG COMPRESSE 98 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429093 - 5 MG COMPRESSE 60 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429117 - 5 MG COMPRESSE 90 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429105 - 5 MG COMPRESSE 84 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429079 - 5 MG COMPRESSE 50 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429081 - 5 MG COMPRESSE 56 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429042 - 5 MG COMPRESSE 20 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429030 - 5 MG COMPRESSE 14 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429028 - 5 MG COMPRESSE 10 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429016 - 5 MG COMPRESSE 7 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429131 - 5 MG COMPRESSE 100 COMPRESSE IN BLISTER PVC/AL - Revocato; 039429067 - 5 MG COMPRESSE 30 COMPRESSE IN BLISTER PVC/AL - Revocato

Autorizācija statuss:

Revocato