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XELEVIA

50MG TBL FLM 90

SÚKL code 0194837
Name of the product XELEVIA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i XELEVIA
Supplement 50MG TBL FLM 90
Strenght 50MG
Pharmaceutical form Film-coated tablet
Package 90
Route Oral use
Wrap type Blister
Legal status na lékařský předpis
Active substance SITAGLIPTIN PHOSPHATE MONOHYDRATE (SITAGLIPTINI PHOSPHAS MONOHYDRICUS)
ATC group A10BH01
ATC group name SITAGLIPTIN

Marketing authorisation information

Registration Number EU/1/07/382/022
Type of MA centralised without orphans
MA status R - active MA/authorised medicinal product
MA Holder Merck Sharp & Dohme B.V., Haarlem
MA Holder country NIZOZEMSKO

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