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ZOLETORV

10MG/10MG TBL FLM 30

SÚKL code 0233458
Name of the product ZOLETORV
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ZOLETORV
Supplement 10MG/10MG TBL FLM 30
Strenght 10MG/10MG
Pharmaceutical form Film-coated tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ATORVASTATIN CALCIUM TRIHYDRATE (ATORVASTATINUM CALCICUM TRIHYDRICUM)
EZETIMIBE (EZETIMIBUM)
ATC group C10BA05
ATC group name ATORVASTATIN A EZETIMIB

Marketing authorisation information

Registration Number 31/ 403/14-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 31. 10. 2022
MA Holder Merck Sharp & Dohme B.V., Haarlem
MA Holder country NIZOZEMSKO
Actual MA holder N.V. Organon, Oss
Actual MA holder country NIZOZEMSKO

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