Details
Product Name in the RMS: TENLORIS 50/10 mg
MR Number: HU/H/0350/002
Date of outcome: 06.01.2014
Type of application | |
---|---|
Level 1: Level 2: Level 3: Level 4: Level 5: |
Known Active Substance Initial Application Fixed Combination Chemical Substance Prescription Only |
Active Substances |
amlodipine besilate 10 mg losartan potassium salt 50 mg |
Form | Film coated tablet |
MA Holder in the RMS |
Krka, d.d., Novo mesto Address: Šmarješka cesta 6, 8501 Novo mesto Country: Slovenia |
RMS | Hungary |
Date of last change | 13.11.2020 |
ATC-Code |
C09DB06 losartan and amlodipine |
CMS Country | Domestic Product Name |
---|---|
Bulgaria | Tenloris |
Estonia | TENLORIS |
Latvia | Tenloris 50 mg/10 mg apvalkotās tabletes |
Lithuania | Tenloris 50 mg/10 mg plėvele dengtos tabletės |
Poland | Alortia |
Romania | TENLORIS 50 mg/10 mg comprimate filmate |
Slovak Republic | Tenloris 50 mg/10 mg filmom obalené tablety |
Documents | |
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PAR: | HU_H_0350_002_PAR.pdf (29.01.2015) |