DOMEPRESS

Valsts: Itālija

Valoda: itāļu

Klimata pārmaiņas: AIFA (Agenzia Italiana del Farmaco)

Nopērc to tagad

Aktīvā sastāvdaļa:

Lisinopril e diuretici

Pieejams no:

GEDEON RICHTER PLC

ATĶ kods:

C09BA03

SNN (starptautisko nepatentēto nosaukumu):

Lisinopril and diuretics

Vienības iepakojumā:

"10 MG/5 MG COMPRESSE" 100 COMPRESSE IN BLISTER PVC/PE/PVDC/AL; "10 MG/5 MG COMPRESSE" 28 COMPRESSE IN BLISTER PVC/PE/PVDC/AL; "

Klase:

M

Ārstniecības joma:

Lisinopril e diuretici

Produktu pārskats:

040614012 - 20 MG/5 MG COMPRESSE 28 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614149 - 20 MG/10 MG COMPRESSE 98 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614164 - 10 MG/5 MG COMPRESSE 28 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614240 - 20 MG/5 MG COMPRESSE 60 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614190 - 10 MG/5 MG COMPRESSE 56 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614099 - 20 MG/10 MG COMPRESSE 30 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614087 - 20 MG/10 MG COMPRESSE 28 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614226 - 10 MG/5 MG COMPRESSE 98 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614075 - 20 MG/5 MG COMPRESSE 100 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614051 - 20 MG/5 MG COMPRESSE 90 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614036 - 20 MG/5 MG COMPRESSE 50 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614137 - 20 MG/10 MG COMPRESSE 90 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614253 - 20 MG/5 MG COMPRESSE 20 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614202 - 10 MG/5 MG COMPRESSE 60 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614152 - 20 MG/10 MG COMPRESSE 100 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614113 - 20 MG/10 MG COMPRESSE 56 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614024 - 20 MG/5 MG COMPRESSE 30 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614188 - 10 MG/5 MG COMPRESSE 50 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614176 - 10 MG/5 MG COMPRESSE 30 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614048 - 20 MG/5 MG COMPRESSE 56 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614214 - 10 MG/5 MG COMPRESSE 90 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614238 - 10 MG/5 MG COMPRESSE 100 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614125 - 20 MG/10 MG COMPRESSE 60 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614101 - 20 MG/10 MG COMPRESSE 50 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato; 040614063 - 20 MG/5 MG COMPRESSE 98 COMPRESSE IN BLISTER PVC/PE/PVDC/AL - Revocato

Autorizācija statuss:

Revocato

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