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KALETRA

200MG/50MG TBL FLM 120

SÚKL code 0167816
Name of the product KALETRA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i KALETRA
Supplement 200MG/50MG TBL FLM 120
Strenght 200MG/50MG
Pharmaceutical form Film-coated tablet
Package 120
Route Oral use
Wrap type Blister
Legal status na lékařský předpis
Active substance RITONAVIR (RITONAVIRUM)
LOPINAVIR (LOPINAVIRUM)
ATC group J05AR10
ATC group name LOPINAVIR A RITONAVIR

Marketing authorisation information

Registration Number EU/1/01/172/008
Type of MA centralised without orphans
MA status R - active MA/authorised medicinal product
MA Holder AbbVie Deutschland GmbH & Co.KG, Ludwigshafen
MA Holder country NĚMECKO

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